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.
Dhanuka, A., Adhikari, A., Agarwala, P., & Mandal, P. K. (2018). Atypical Mayer–Rokitansky–Kuster–Hauser syndrome − report of a rare case. Kasr Al Ainy Medical Journal, 24(3), -. doi: 10.4103/kamj.kamj_11_18
MLA
Ankita Dhanuka; Anindya Adhikari; Priyanka Agarwala; Palash K. Mandal. "Atypical Mayer–Rokitansky–Kuster–Hauser syndrome − report of a rare case". Kasr Al Ainy Medical Journal, 24, 3, 2018, -. doi: 10.4103/kamj.kamj_11_18
HARVARD
Dhanuka, A., Adhikari, A., Agarwala, P., Mandal, P. K. (2018). 'Atypical Mayer–Rokitansky–Kuster–Hauser syndrome − report of a rare case', Kasr Al Ainy Medical Journal, 24(3), pp. -. doi: 10.4103/kamj.kamj_11_18
VANCOUVER
Dhanuka, A., Adhikari, A., Agarwala, P., Mandal, P. K. Atypical Mayer–Rokitansky–Kuster–Hauser syndrome − report of a rare case. Kasr Al Ainy Medical Journal, 2018; 24(3): -. doi: 10.4103/kamj.kamj_11_18
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