Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5α-Reductase Type 2 Deficiency

The aim of this study was to search for clinical and laboratorial data in 46,XY patients with ambiguous genitalia (AG) and normal testosterone (T) synthesis that could help to distinguish partial androgen insensitivity syndrome (PAIS) from 5α-reductase type 2 deficiency (5α-RD2) and from cases witho...

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Main Authors: Veiga-Junior, Nélio Neves, Medaets, Pedro Augusto Rodrigues, Petroli, Reginaldo José, Calais, Flávia Leme, de Mello, Maricilda Palandi, Castro, Carla Cristina Telles de Sousa, Guaragna-Filho, Guilherme, Sewaybricker, Letícia Espósito, Marques-de-Faria, Antonia Paula, Maciel-Guerra, Andréa Trevas, Guerra-Junior, Gil
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2012
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3238364/
https://ncbi.nlm.nih.gov/pubmed/22194745
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/964876
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