A rare case of 46,XX gonadal dysgenesis, Mayer–Rokitansky–Kuster–Hauser syndrome, pituitary and thyroid hypoplasia

SUMMARY: Mayer–Rokitansky–Kuster–Hauser syndrome is characterized by congenital absence or hypoplasia of the uterus and upper two-thirds of the vagina in both phenotypically and karyotypically normal females with functional ovaries, whereas gonadal dysgenesis is a primary ovarian defect in otherwise...

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Detalles Bibliográficos
Autores principales: Ambachew, Rediet, Gulilat, Amare, Aberra, Tewodros, Terefework, Zewdu, Bedilu, Wubalem, Tarekegn, Getahun, Reja, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8859947/
https://www.ncbi.nlm.nih.gov/pubmed/35142292
http://dx.doi.org/10.1530/EDM-21-0103

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8859947/
https://www.ncbi.nlm.nih.gov/pubmed/35142292
http://dx.doi.org/10.1530/EDM-21-0103

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