非性行為傳染 女大生得菜花 http://www.flickr.com/photos/85944727@N00/4810109843/ http://www.youtube.com/watch?v=ChECsUn-edk
http://www.libertytimes.com.tw/2010/new/jul/20/today-health4.htm http://www.youtube.com/watch?v=mx0BOZcECzY 記者吳為恭/彰化報導
非性行為傳染 女大生得菜花http://www.libertytimes.com.tw/2010/new/jul/20/today-health4.htm 記者吳為恭/彰化報導 2010-7-20字型: ∣看推薦∣發言∣列印∣轉寄∣分享:非性行為傳染 女大生得菜花http://www.libertytimes.com.tw/2010/new/jul/20/today-health4.htm 記者吳為恭/彰化報導一名清秀女大學生被診斷出罹患性病「菜花」後流淚表示,她只有一個男朋友,怎會得「菜花」?懷疑是男友濫交惹禍,但經過檢查,她的男友並沒有感染到人類乳突病毒(HPV);醫師說,HPV有可能透過「非性行為」感染。博元婦產科院長蔡鋒博表示,「菜花」的醫學名詞是尖圭濕疣,也叫陰部濕疣或性濕疣,一般發生在口腔、肛門及生殖器。發生在生殖器者大部分是經由性行為感染HPV引起,以HPV6型、HPV11型最普遍,但是也有可能從觸摸到公共場所的不潔把手、水龍頭等處,感染到HPV。一度懷疑男友濫交蔡鋒博指出,這名女大學生之外,也有一位人妻被驗出子宮頸感染HPV,氣沖沖地拉著丈夫到醫院做HPV的DNA晶片檢查,在丈夫的生殖器龜頭上採樣,結果丈夫並無她所感染的那一類型HPV,患者才氣消。蔡鋒博說,要預防感染HPV病毒,除了注意安全性行性為,不濫交之外,但是比較難防範在公共場所因接觸感染到HPV病毒的情形,只能靠勤用肥皂洗手,或是接種HPV疫苗等方式預防。 博元婦產科不孕症試管嬰兒中心:蔡鋒博醫師,陳昭雯醫師博元婦產科不孕症試管嬰兒中心:蔡鋒博醫師,陳昭雯醫師客服電話:0911905889 地址: 50044 彰化市中正路1段392號
- Jul 20 Tue 2010 16:53
非性行為傳染 女大生得菜花
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- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR 目前顯示的是「博元-一條龍海報更新版3.jpg」目前顯示的是「博元-一條龍海報更新版3.jpg」 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone 彰化市 博元婦產科 蔡鋒博 醫師
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR 目前顯示的是「博元-一條龍海報更新版3.jpg」目前顯示的是「博元-一條龍海報更新版3.jpg」 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone 博元婦產科蔡鋒博陳昭雯醫師 http://www.babymaker.com.tw/ 博元youtube:http://goo.gl/DFOL2r 博元手機APP: http://goo.gl/NOyhFd到以下網址,就是博元手機APP手機版網頁app:http://goo.gl/NOyhFd,下載、安裝博元婦產科助妳好孕大全集盡在優酷網http://goo.gl/w1Un0k 成為 博元臉書粉絲 : http://www.facebook.com/yes7260678 蔡醫師-門診表 :週一至週五下午、晚上& 週六全天 陳醫師-門診表:週一至週五早上 電話:04-7260678 Fax: 04-7225626 e-mail: ok7260678@gmail.com 掛號專線:04-7260678 (ext:111;112)地址: 彰化市中正路1段392號 MAP: http://goo.gl/tp3rEE 博元 Address:500; 392 Zhong Zheng Road ,Sec.1 ,Chang-Hua ,Taiwan 到博元婦產科最快的方法是坐國光號http://goo.gl/bsm7uQ Address:500; 392 Zhong Zheng Road ,Sec.1 ,Chang-Hua ,Taiwan 您搭高鐵怎麼到博元婦產科?see-http://www.youtube.com/watch?v=CQ163SfmN4s 坐火車如何"走到"博元婦產科?http://goo.gl/SNjhV2 ubike到博元婦產科:http://goo.gl/BZBX4X 博元婦產科官方Youtube http://goo.gl/6UTLeV 博元婦產科官方部落格http://hi7250567.blogspot.com/ 博元婦產科Twitter: http://twitter.com/7260678 博元婦產科官方flickr http://www.flickr.com/photos/85944727@N00/ 博元google+:google.com/+彰化博元婦產科https://plus.google.com/114810735851376657250/about?cfem=1 https://plus.google.com/114810735851376657250/about?cfem=1來博元婦產科,停車場在哪?(1)http://www.youtube.com/watch?v=Xeg5JDmRwyc(2) http://www.youtube.com/watch?v=AOa-oC7cOMQ 博元婦產科 Line ID:047260678 博元婦產科微信 ID :ok7260678 請用臉書的即時通 FB messanger 和博元婦產科聯絡
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR 目前顯示的是「博元-一條龍海報更新版3.jpg」目前顯示的是「博元-一條龍海報更新版3.jpg」 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR 目前顯示的是「博元-一條龍海報更新版3.jpg」目前顯示的是「博元-一條龍海報更新版3.jpg」 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR 目前顯示的是「博元-一條龍海報更新版3.jpg」目前顯示的是「博元-一條龍海報更新版3.jpg」 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR 目前顯示的是「博元-一條龍海報更新版3.jpg」目前顯示的是「博元-一條龍海報更新版3.jpg」 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR 目前顯示的是「博元-一條龍海報更新版3.jpg」目前顯示的是「博元-一條龍海報更新版3.jpg」 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone 彰化市 博元婦產科 蔡鋒博 醫師.發自iPhone
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR
- 2015: 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 一條龍試管嬰兒研究論文報告發表在分子細胞遺傳學2015年7月8日 胚胎快篩一條龍試管嬰兒,新鮮胚胎植入的PGS研究論文報告發表了, 博元婦產科和彰基基因醫學部共同的研究報告,使用qPCR進行PGS進行新鮮胚胎植入,論文發表在分子細胞遺傳學2015年7月8日,在PUBMED就可以找到這份論文,請看以下報告: Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Mol Cytogenet. 2015 Jul 8;8:49. doi: 10.1186/s13039-015-0140-9. eCollection 2015. Yang YS1, Chang SP2, Chen HF3, Ma GC4, Lin WH2, Lin CF1, Tsai FP5, Wu CH6, Tsai HD6, Lee TH7, Chen M8. Author information 1Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan. 2Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan. 3Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. 4Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan. 5Poyuan Women Clinic, Changhua, Taiwan. 6Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan. 7Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Obstetrics and Gynecology, Chung-Shan Medical University, Taichung, Taiwan. 8Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan ; Department of Genomic Medicine, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan ; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan ; Department of Life Sciences, Tunghai University, Taichung, Taiwan. Abstract BACKGROUND: Aneuploidy is an important e tiology of implantation failure and quantitative real-time polymerase chain reaction (qPCR) seems a promising preimplantation genetic screening (PGS) technology to detect aneuploidies. This verification study aimed at verifying the impact on reproductive outcomes in in vitro fertilization (IVF) cycles using fresh embryo transfer (FET) in which the embryos were selected by blastocyst biopsy with qPCR-based PGS in our settings. RESULTS: A total of 13 infertile couples with more than once failed in vitro fertilization were enrolled during July to October of 2014. PGS was conducted by qPCR with selectively amplified markers to detect common aneuploidies (chromosomes 13, 18, 21, X, and Y). The design of the qPCR molecular markers adopted the locked nucleic acid (LNA) strategy. The blastocyst biopsy was performed on Day 5/6 and the PGS was done on the same day, which enabled FET. A total of 72 blastocysts were biopsied. Successful diagnoses were established in all embryos and the rate of successful diagnosis was 100 %. The aneuploidy rate was 38.9 % (28/72). 28 embryos were transferred. The clinical pregnancy rate was 61.5 % (8/13) per cycle. Early first trimester abortion was encountered in 1 and the ongoing pregnancy rate was 53.8 % (7/13) per cycle. CONCLUSION: This study verified the favorable outcome of adopting PGS with qPCR + FET in our own setting. Expanding the repertoire of aneuploidies being investigated (from a limited set to all 24 chromosomes) is underway and a randomized study by comparing qPCR and other PGS technologies is warranted. KEYWORDS: Aneuploidy; Blastocyst; Fresh embryo transfer; PGS; qPCR
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