| Literature DB >> 27832414 |
Diogo C Soares1, Mariana N Stroparo2, Yu C Lian2, Cristina Y Takakura3, Sabrina Wolf4, Regina Betz4, Chong A Kim5.
Abstract
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.Entities:
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Year: 2016 PMID: 27832414 DOI: 10.1007/s10545-016-9996-z
Source DB: PubMed Journal: J Inherit Metab Dis ISSN: 0141-8955 Impact factor: 4.982