Atypical Mayer–Rokitansky–Kuster–Hauser syndrome − report of a rare case | ||||
Kasr Al Ainy Medical Journal | ||||
Volume 24, Issue 3, September 2018 PDF (909.16 K) | ||||
DOI: 10.4103/kamj.kamj_11_18 | ||||
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Authors | ||||
Ankita Dhanuka; Anindya Adhikari; Priyanka Agarwala; Palash K. Mandal | ||||
Abstract | ||||
Mayer–Rokitansky–Kuster–Hauser syndrome is a rare disorder affecting 1 in 5000 women. It is characterized by congenital absence of the uterus and the vagina in a phenotypically and karyotypically normal female. Here, we report a case of atypical Mayer–Rokitansky–Kuster–Hauser in a 13-year-old girl who also had abnormalities in the ovaries. | ||||
Keywords | ||||
ATYPICAL; Mayer–Rokitansky–Kuster–Hauser syndrome; mullerian ageanesis | ||||
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