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Indian J Pediatr ; 2005 Aug; 72(8): 701-3
Artigo em Inglês | IMSEAR | ID: sea-82707

RESUMO

Branchio-oculo-facial syndrome (BOFS) is a very rare autosomal dominant disorder with incomplete penetrance and variable expression; with phenotypic variation ranging from mild to severe forms, involving eye, ear, oral and craniofacial structure. We report three members of one family, showing great variability in its phenotypic expression and review the recent literature.


Assuntos
Adolescente , Síndrome Brânquio-Otorrenal/diagnóstico , Criança , Feminino , Genes Dominantes , Humanos , Masculino , Fenótipo
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