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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238364/
https://www.ncbi.nlm.nih.gov/pubmed/22194745
http://dx.doi.org/10.1155/2012/964876

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238364/
https://www.ncbi.nlm.nih.gov/pubmed/22194745
http://dx.doi.org/10.1155/2012/964876

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