Nonclassic Congenital Adrenal Hyperplasia

Nonclassic congenital adrenal hyperplasia (NCAH) due to P450c21 (21-hydroxylase deficiency) is a common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 gene which is located at chromosome 6p21. The clinical features predominantly reflect androgen excess rather than adr...

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Detalles Bibliográficos
Autores principales: Witchel, Selma Feldman, Azziz, Ricardo
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910408/
https://www.ncbi.nlm.nih.gov/pubmed/20671993
http://dx.doi.org/10.1155/2010/625105

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910408/
https://www.ncbi.nlm.nih.gov/pubmed/20671993
http://dx.doi.org/10.1155/2010/625105

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