Premature Moustache As Presenting Symptom of Nonclassic Congenital Adrenal Hyperplasia due to 2 Uncommon Mutations of the CYP21A2 Gene

A Turkish boy was referred at the age of 3 6/12 years for the evaluation of a premature moustache. No other signs of virilisation were present. The endocrine evaluation led to the diagnosis of nonclassic congenital adrenal hyperplasia. Genetic analysis revealed 2 rare mutations of the CYP21A2 gene,...

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Detalles Bibliográficos
Autores principales: Massa, Guy, Gillis, Philippe, Schwartz, Marianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447225/
https://www.ncbi.nlm.nih.gov/pubmed/23074682
http://dx.doi.org/10.1155/2011/913020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447225/
https://www.ncbi.nlm.nih.gov/pubmed/23074682
http://dx.doi.org/10.1155/2011/913020

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