AB079. Phenotype variation in untreated 46,XX congenital adrenal hyperplasia

Simple virilizing congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder characterized by 21 hydroxylase deficiency leading to excessive androgen production. In infants with 46,XX karyotype, prenatal exposure of androgen overproduction leads to a gradual virilization of the external...

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Detalles Bibliográficos
Publicado en:Ann Transl Med
Main Authors: Faradz, Sultana MH, Utari, Agustini, Ediati, Annastasia, Ariani, Mahayu Dewi, Juniarto, Achmad Zulfa
Formato: Artigo
Idioma:Inglês
Publicado: AME Publishing Company 2015
Assuntos:
Part 4: Oral/poster
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563431/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB079
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