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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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Bibliografiska uppgifter
I publikationen:Ann Transl Med
Huvudupphovsmän: Faradz, Sultana MH, Utari, Agustini, Ediati, Annastasia, Ariani, Mahayu Dewi, Juniarto, Achmad Zulfa
Materialtyp: Artigo
Språk:Inglês
Publicerad: AME Publishing Company 2015
Ämnen:
Länkar: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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