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Artigo em Inglês | IMSEAR | ID: sea-156324

RESUMO

Biotinidase deficiency is a rare metabolic disorder which can cause dermatological manifestations and lead to severe neurological sequelae if untreated. Holocarboxylase synthetase deficiency also has similar manifestations and needs to be differentiated. We present a neonate who had atypical early onset symptoms and was diagnosed to have biotinidase deficiency.


Assuntos
Alopecia/etiologia , Deficiência de Biotinidase/complicações , Deficiência de Biotinidase/diagnóstico , Deficiência de Biotinidase/genética , Evolução Fatal , Feminino , Humanos , Ictiose/etiologia , Recém-Nascido , Convulsões/etiologia
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