| Literature DB >> 7844676 |
L G Rabinowitz1, L R Williams, C E Anderson, A Mazur, P Kaplan.
Abstract
Tyrosinemia type II (Richner-Hanhart syndrome), which is caused by a deficiency of hepatic tyrosine aminotransferase, results in elevated plasma and urinary tyrosine concentrations. We describe a young boy who was seen at 6 months of age with red eyes, photophobia, and eye pain that were not suspected to be caused by tyrosinemia II until painful plantar keratoderma developed at 2 1/2 years of age. Treatment with a diet low in tyrosine and phenylalanine reversed the manifestations of the disease.Entities:
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Year: 1995 PMID: 7844676 DOI: 10.1016/s0022-3476(95)70558-9
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406