Phenotypic variability of hyperandrogenemia in females heterozygous for CYP21A2 mutations

OBJECTIVES: The objective was to seek evidence on the prevalence and consequences of heterozygous CYP21A2 mutations in girls, adolescent, and adult females with clinical manifestation of androgen excess. PATIENTS AND METHODS: The study included 64 girls diagnosed with premature adrenarche (PA) in ch...

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Detalhes bibliográficos
Publicado no:Indian J Endocrinol Metab
Main Authors: Neocleous, Vassos, Shammas, Christos, Phedonos, Alexia AP, Phylactou, Leonidas A, Skordis, Nicos
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2014
Assuntos:
Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4266872/
https://ncbi.nlm.nih.gov/pubmed/25538881
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.145077
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