Azoospermia in a Male with Klippel–Feil Anomaly

Maria Uloko; Elizabeth Bearrick; Joshua Bodie

doi:10.1016/j.eucr.2017.03.007

Azoospermia in a Male with Klippel–Feil Anomaly

Maria Uloko, Elizabeth Bearrick, Joshua Bodie

Urology

Research output: Contribution to journal › Article › peer-review

Abstract

Müllerian-duct aplasia, renal agenesis, and cervical somite dysplasia (MURCS) is a rare genetic disorder. Previously thought to be exclusive in females, there have now been a small number of case reports describing a male analogue. We describe a patient with obstructive azoospermia and Klippel–Feil anomaly.

Original language	English (US)
Pages (from-to)	51-52
Number of pages	2
Journal	Urology Case Reports
Volume	13
DOIs	https://doi.org/10.1016/j.eucr.2017.03.007
State	Published - Jul 1 2017

Bibliographical note

Publisher Copyright:
© 2017

Keywords

Cervical somite dysplasia
Infertility
Klippel Feil anomaly
Mullerian duct aplasia
Renal agenesis

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10.1016/j.eucr.2017.03.007

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407570

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AB - Müllerian-duct aplasia, renal agenesis, and cervical somite dysplasia (MURCS) is a rare genetic disorder. Previously thought to be exclusive in females, there have now been a small number of case reports describing a male analogue. We describe a patient with obstructive azoospermia and Klippel–Feil anomaly.

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KW - Infertility

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KW - Renal agenesis

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Azoospermia in a Male with Klippel–Feil Anomaly

Abstract

Bibliographical note

Keywords

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