Painful keratoderma and photophobia: hallmarks of tyrosinemia type II.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 7844676.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
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.
Medical subject headings
- Amino Acid Metabolism, Inborn Errors
- Keratoderma, Palmoplantar
- Light
- Tyrosine