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Male Gender Identity and Reversible Hypokalemic Hypertension in a 46,XX Child with 11-Beta-Hydroxylase Deficiency Congenital Adrenal Hyperplasia

Steroid 11-beta-hydroxylase deficiency is a relatively rare form of congenital adrenal hyperplasia (CAH). We describe the case of a 46,XX child, reared as a male, who first presented to us at the age of three years with features of peripheral precocity and hypokalemic hypertension. Based on the clin...

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Pubblicato in:Cureus
Autori principali: Goyal, Alpesh, Boro, Hiya, Khadgawat, Rajesh
Natura: Artigo
Lingua:Inglês
Pubblicazione: Cureus 2019
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6760881/
https://ncbi.nlm.nih.gov/pubmed/31572633
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.5248
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