Manne, S., Veeraabhinav, H., Jett, M., Himabindu, Y., Donthu, K. and Badireddy, M. (2016) A Rare Case of 46, XX Gonadal Dygenesis and Mayer-Rokitansky-Kuster-Hauser Syndrome. Journal of Human Reproductive Sciences, 9, 263-266.
https://doi.org/10.4103/0974-1208.197694

has been cited by the following article:

• TITLE: Case Report: Clinical and Diagnostic Aspects of Mayer-Rokitansky-Kuster-Hauser Syndrome

  AUTHORS: Lucas Ferreira de Paula Filho, Guilherme Carolino Neves, Laís Figueira Bandoli, Lucas Caraline de Almeida Coelho, Nathália de Souza Ferreira Feital, Renan Vieira Murad, Ana Luísa Conceição de Jesus, Diana Aristótelis de Sá, Larissa Bianca Cunha de Sá, Jonathan Mwambire, Alberto Krayyem Arbex

  KEYWORDS: Mayer-Rokitansky-Kuster-Hauser Syndrome, Primary Amenorrhea, Gonadal Dysgenesis

  JOURNAL NAME: Health, Vol.11 No.10, October 22, 2019

  ABSTRACT: Mayer-Rokitansky-Kuster-Hauser Syndrome (MRKH) is a rare disease characterized by total or partial vagina agenesis, karyotype 46, XX with normal secondary sexual characters. Still, it is the second leading cause of primary amenorrhea. The absence of obvious signs and symptoms often causes the syndrome to be diagnosed only after puberty. The case presented here highlights exactly this difficulty of early diagnosis, which meets the objective of the study, and is precisely to provide reliable material that facilitates the diagnosis and management of patients with MRKH syndrome.