Rokitansky kuster hauser syndrome

A rare syndrome of unknown cause that occurs in females. It is characterized by underdeveloped or absent vagina and uterus in an otherwise phenotypically normal female with a normal 46,XX karyotype. Other abnormalities include unilateral renal agenesis, skeletal abnormalities, hearing loss, and heart defects.

Disease Alternative Name

mullerian aplasia/dysgenesis
mayer-rokitansky-kuster-hauser syndrome
mrkh syndrome
mrkh
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M.D In Gynec at B.J.M.C A'bad.2003

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, M.Ch Ped Surgery KGMU Lucknow 2012 2015

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