Cargando…

A rare case of 46,XX gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome

46,XX gonadal dysgenesis is a rare genetically heterogeneous disorder characterized by underdeveloped ovaries with consequent, impuberism, primary amenorrhea, and hypergonadotropic hypogonadism. Mullerian agenesis or Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by congenital aplas...

Descripción completa

Detalles Bibliográficos
Autores principales: Manne, Sriharibabu, Veeraabhinav, C. H., Jetti, Mounica, Himabindu, Yalamanchali, Donthu, Kiranmai, Badireddy, Mutyalarayudu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5296832/
https://www.ncbi.nlm.nih.gov/pubmed/28216916
http://dx.doi.org/10.4103/0974-1208.197694