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Endocrinol Nutr ; 56(8): 428-30, 2009 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-19959154

RESUMO

Pendred's syndrome is an autosomal recessive disorder leading to congenital sensorineural hearing loss and a variable degree of goiter due to reduced iodine organification. The cause of this disease is dysfunction of an anion transporter protein located on the apical membrane of thyrocytes, called pendrin, which is also found in the kidney and cochlea. Molecular analysis of the gene is useful to identify other affected family members and provide proper genetic advice and early diagnosis in descendants. We present the cases of two siblings with sensorineural deafness who were diagnosed with Pendred's syndrome as adults because one of them consulted for goiter.


Assuntos
Bócio/genética , Perda Auditiva Neurossensorial/genética , Proteínas de Membrana Transportadoras/genética , Adulto , Transporte Biológico/genética , Endolinfa/metabolismo , Genes Recessivos , Perda Auditiva Neurossensorial/congênito , Humanos , Achados Incidentais , Rim/metabolismo , Masculino , Proteínas de Membrana Transportadoras/fisiologia , Transportadores de Sulfato , Síndrome , Glândula Tireoide/metabolismo
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