The Richner-Hanhart Syndrome
- 1 July 1976
- journal article
- case report
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 94 (7) , 1133-1137
- https://doi.org/10.1001/archopht.1976.03910040045009
Abstract
• The Richner-Hanhart syndrome with tyrosinemia was recognized in a mentally retarded adolescent boy. The clinical manifestations, including hyperkeratosis of the volar aspects of the hands and feet, thickening of the conjunctival epithelium, and corneal opacities, as well as biochemical aberrations of tyrosine metabolism, responded to specific treatment with a diet low in phenylalanine and tyrosine. Light and electron microscopical studies illustrate the underlying conjunctival pathologic changes.Keywords
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- Soluble Tyrosine Aminotransferase Deficiency: An Unusual Cause of Corneal UlcersAmerican Journal of Ophthalmology, 1972
- Metabolic Studies in a Patient with Hepatic Cytosol Tyrosine Aminotransferase DeficiencyPediatric Research, 1971
- Tyrosinosis: biochemical studies of an unusual caseClinical Biochemistry, 1971