Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome Type 2: Atypical Presentation of Rare Case

摘要

Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital malformation characterized by an absence of the vagina associated with a variable abnormality of the uterus and the urinary tract but functional ovaries. We are reporting atypical presentation of rare case. Patient had obstructed left inguinal hernia with genitourinary and skeletal deformity. Latter it diagnosed as Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome which is a rare disease.