Wordt geladen...

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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Gepubliceerd in:Ann Transl Med
Hoofdauteurs: Faradz, Sultana MH, Utari, Agustini, Ediati, Annastasia, Ariani, Mahayu Dewi, Juniarto, Achmad Zulfa
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: AME Publishing Company 2015
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563431/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB079
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!