Pseudohermaphroditism due to XY gonadal absence syndrome.

A 21-year-old phenotypic female with a 46,XY chromosome complement and gonadal absence was studied. Basal levels of plasma immunoreactive luteinizing hormone (LH), follicle stimulating hormone (FSH), testosterone, and oestradiol were measured. Pituitary sensitivity and reserve was evaluated by the e...

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Hauptverfasser: Alfaro, S K, Saavedra, D, Ochoa, S, Scaglia, H, Pérez-Palacios, G
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1976
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1013402/
https://ncbi.nlm.nih.gov/pubmed/933126
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