Volume : VI, Issue : IV, April - 2017

A RARE CASE OF ANDROGEN INSENSITIVITY SYNDROME WITH BILATERAL GONADOBLASTOMA

Bankat Phad, Zeeba Usofi, Mohan Joshi

Abstract :

 AIS is a rare inherited form of male pseudohermaphroditism that can manifest as a normal female phenotype without müllerian derivatives and absence of the upper third of the vagina.[1] The androgen insensitivity syndrome (AIS) is a disease connected with the inactivation of AR due to a mutation that inactivates male sexual differentiation, and causes a spectrum of phenotypic anomalies having as a common aspect the loss of reproductive characteristics.[2] The androgen insensitivity syndrome occurs in one out of 20,000 births and can be incomplete (various sexual ambiguities) or complete (the person appears to be a woman < clear="all" style="page–eak–before:always; mso–eak–type:section–eak" />

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Article: Download PDF   DOI : 10.36106/ijsr  

Cite This Article:

Bankat Phad, Zeeba Usofi, Mohan Joshi, A RARE CASE OF ANDROGEN INSENSITIVITY SYNDROME WITH BILATERAL GONADOBLASTOMA, INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : VOLUME-6 | ISSUE-4 | APRIL‾2017

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