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Indian J Pediatr ; 2006 Feb; 73(2): 161-2
Artigo em Inglês | IMSEAR | ID: sea-81531

RESUMO

Richner Hanhart syndrome is a rare inherited disorder involving the metabolism of tyrosine, a semi-essential amino acid and it should be considered in the differential diagnosis of a child presenting with ocular and skin lesions. We report a case of Richner Hanhart syndrome in a 19-month-old child, who presented with ocular and skin lesions.


Assuntos
Oftalmopatias/etiologia , Feminino , Humanos , Lactente , Dermatopatias/etiologia , Tirosinemias/complicações
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