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Sertoli cell only syndrome with ambiguous genitalia.

作者信息

Gurbuz Fatih, Ceylaner Serdar, Erdogan Seyda, Topaloglu Ali Kemal, Yuksel Bilgin

出版信息

J Pediatr Endocrinol Metab. 2016 Jul 1;29(7):849-52. doi: 10.1515/jpem-2015-0458.

DOI:10.1515/jpem-2015-0458
PMID:27124672
Abstract

The Sertoli cell only syndrome (SCOS) is a rare genetic disorder with a variable phenotype ranging from a severe ambiguous genitalia to a normal male phenotype with infertility. SCOS is diagnosed on testicular histopathology as germ cells are absent without histological impairment of Sertoli or Leydig cells. The SRY positive XX male syndrome is usually diagnosed in adulthood during infertility investigations. Here, we report a rare case of 46,XX maleness with ambiguous genitalia due to Sertoli cell only syndrome (SCOS).

摘要

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