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J Inherit Metab Dis ; 40(3): 461-462, 2017 05.
Artículo en Inglés | MEDLINE | ID: mdl-27832414

RESUMEN

Richner-Hanhart syndrome (RHS, tyrosinemia type II) is a rare, autosomal recessive inborn error of tyrosine metabolism caused by tyrosine aminotransferase deficiency. It is characterized by photophobia due to keratitis, painful palmoplantar hyperkeratosis, variable mental retardation, and elevated serum tyrosine levels. Patients are often misdiagnosed with herpes simplex keratitis. We report on a a boy from Brazil who presented with bilateral keratitis secondary to RHS, which had earlier been misdiagnosed as herpes simplex keratitis.


Asunto(s)
Queratitis/diagnóstico , Queratodermia Palmoplantar/diagnóstico , Tirosinemias/diagnóstico , Brasil , Preescolar , Humanos , Masculino
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