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An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis

We report the case of a 46-year-old Chinese male patient who visited our clinic complaining of infertility. Semen analysis revealed azoospermia, and azoospermia factor c region partial deletion (b1/b3) was detected using Y chromosome microdeletion analysis. Testicular sperm extraction was performed...

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Autores principales: Kuroda, Shinnosuke, Usui, Kimitsugu, Mori, Kohei, Yasuda, Kengo, Asai, Takuo, Sanjo, Hiroyuki, Yakanaka, Hiroyuki, Takeshima, Teppei, Kawahara, Takashi, Hamanoue, Haruka, Kato, Yoshitake, Miyoshi, Yasuhide, Uemura, Hiroji, Iwasaki, Akira, Yumura, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Reproductive Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897248/
https://www.ncbi.nlm.nih.gov/pubmed/29662826
http://dx.doi.org/10.5653/cerm.2018.45.1.48
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author Kuroda, Shinnosuke
Usui, Kimitsugu
Mori, Kohei
Yasuda, Kengo
Asai, Takuo
Sanjo, Hiroyuki
Yakanaka, Hiroyuki
Takeshima, Teppei
Kawahara, Takashi
Hamanoue, Haruka
Kato, Yoshitake
Miyoshi, Yasuhide
Uemura, Hiroji
Iwasaki, Akira
Yumura, Yasushi
author_facet Kuroda, Shinnosuke
Usui, Kimitsugu
Mori, Kohei
Yasuda, Kengo
Asai, Takuo
Sanjo, Hiroyuki
Yakanaka, Hiroyuki
Takeshima, Teppei
Kawahara, Takashi
Hamanoue, Haruka
Kato, Yoshitake
Miyoshi, Yasuhide
Uemura, Hiroji
Iwasaki, Akira
Yumura, Yasushi
author_sort Kuroda, Shinnosuke
collection PubMed
description We report the case of a 46-year-old Chinese male patient who visited our clinic complaining of infertility. Semen analysis revealed azoospermia, and azoospermia factor c region partial deletion (b1/b3) was detected using Y chromosome microdeletion analysis. Testicular sperm extraction was performed after genetic counseling. The bilateral ductus deferens and a portion of the epididymis were absent, whereas the remaining epididymis was expanded. Motile intratesticular spermatozoa were successfully extracted from the seminiferous tubule. On histopathology, nearly complete spermatogenesis was confirmed in almost every seminiferous tubule. To our knowledge, this is the first case report of b1/b3 deletion with a congenital bilateral absence of the vas deferens and almost normal spermatogenesis.
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spelling pubmed-58972482018-04-16 An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis Kuroda, Shinnosuke Usui, Kimitsugu Mori, Kohei Yasuda, Kengo Asai, Takuo Sanjo, Hiroyuki Yakanaka, Hiroyuki Takeshima, Teppei Kawahara, Takashi Hamanoue, Haruka Kato, Yoshitake Miyoshi, Yasuhide Uemura, Hiroji Iwasaki, Akira Yumura, Yasushi Clin Exp Reprod Med Case Report We report the case of a 46-year-old Chinese male patient who visited our clinic complaining of infertility. Semen analysis revealed azoospermia, and azoospermia factor c region partial deletion (b1/b3) was detected using Y chromosome microdeletion analysis. Testicular sperm extraction was performed after genetic counseling. The bilateral ductus deferens and a portion of the epididymis were absent, whereas the remaining epididymis was expanded. Motile intratesticular spermatozoa were successfully extracted from the seminiferous tubule. On histopathology, nearly complete spermatogenesis was confirmed in almost every seminiferous tubule. To our knowledge, this is the first case report of b1/b3 deletion with a congenital bilateral absence of the vas deferens and almost normal spermatogenesis. The Korean Society for Reproductive Medicine 2018-03 2018-03-30 /pmc/articles/PMC5897248/ /pubmed/29662826 http://dx.doi.org/10.5653/cerm.2018.45.1.48 Text en Copyright © 2018. The Korean Society for Reproductive Medicine http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kuroda, Shinnosuke
Usui, Kimitsugu
Mori, Kohei
Yasuda, Kengo
Asai, Takuo
Sanjo, Hiroyuki
Yakanaka, Hiroyuki
Takeshima, Teppei
Kawahara, Takashi
Hamanoue, Haruka
Kato, Yoshitake
Miyoshi, Yasuhide
Uemura, Hiroji
Iwasaki, Akira
Yumura, Yasushi
An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis
title An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis
title_full An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis
title_fullStr An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis
title_full_unstemmed An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis
title_short An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis
title_sort infertile patient with y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897248/
https://www.ncbi.nlm.nih.gov/pubmed/29662826
http://dx.doi.org/10.5653/cerm.2018.45.1.48
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