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
Top Rokitansky kuster hauser syndrome Doctors on Curofy
Top doctors who continously share their opinions on Rokitansky kuster hauser syndromeAssociatec Professor.
M.P.SHAH MEDICAL COLLEAGE
M.D In Gynec at B.J.M.C A'bad.2003
M.D
New Katurba Hospital, Manipal
Intern
Kasturba Medical College, Manipal
MBBS
Govt Nizamia Tibbi College
MD
Senior Resident
, M.Ch Ped Surgery KGMU Lucknow 2012 2015
Kgmu
M.Ch
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