Coexistence of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome in 46, XX female: A case report and review of literature

The association of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome is very rare. We report a 21-year-old phenotypical female who presented with primary amenorrhea and underdeveloped secondary sexual characteristics. Hormonal evaluation revealed hypergonadotropic hypogonadism. Her kary...

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Detalles Bibliográficos
Autores principales: Shah, Viral N., Ganatra, Parth J., Parikh, Rajni, Kamdar, Panna, Baxi, Seema, Shah, Nishit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830331/
https://www.ncbi.nlm.nih.gov/pubmed/24251185
http://dx.doi.org/10.4103/2230-8210.119605

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830331/
https://www.ncbi.nlm.nih.gov/pubmed/24251185
http://dx.doi.org/10.4103/2230-8210.119605

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