Divergent gender identity in three siblings with 46XX karyotype and severely virilizing congenital adrenal hyperplasia caused by a novel CYP11B1 mutation.

Bin-Abbas, Bassam; Al-Humaida, Doha; Al-Sagheir, Afaf; Qasem, Ebtesam; Almohanna, Mai; Alzahrani, Ali S

Bin-Abbas, Bassam; Al-Humaida, Doha; Al-Sagheir, Afaf; Qasem, Ebtesam; Almohanna, Mai; Alzahrani, Ali S.

Afiliação

Bin-Abbas B; Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Al-Humaida D; Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Al-Sagheir A; Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Qasem E; Department of Molecular Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Almohanna M; Department of Molecular Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Alzahrani AS; Department of Molecular Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia Department of Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

Endocr Pract ; 20(10): e191-7, 2014 Oct.

Article em En | MEDLINE | ID: mdl-25100385

Assuntos

Hiperplasia Suprarrenal Congênita; Identidade de Gênero; Esteroide 11-beta-Hidroxilase/genética; Adolescente; Criança; Feminino; Humanos; Cariótipo; Masculino; Mutação; Irmãos

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esteroide 11-beta-Hidroxilase / Hiperplasia Suprarrenal Congênita / Identidade de Gênero Idioma: En Ano de publicação: 2014 Tipo de documento: Article

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