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Article

Complete androgen insensitivity syndrome and discordant Müllerian remnants: two cases with novel mutation in the androgen receptor.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Jan 2013

Güven Ayla, Dursun Fatma, Özkanlı Seyma, Güçlüer Berrin, Kuru L İhsan

Abstract excerpt

Complete androgen insensitivity syndrome (CAIS) associated with Müllerian remnant is rare during childhood. The Müllerian system usually regresses because of the presence of the anti-Müllerian hormone (AMH) originating from the Sertoli cells of the gonads. Rarely, residual Müllerian structures may exist. We present two cases from the same family, raised as females. They were 12 and 18 years old, respectively, and...

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Identifiers

PMID: 23729616
DOI: 10.1515/jpem-2013-0047

Genes

AMH

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