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J Pediatr ; 126(2): 266-9, 1995 Feb.
Article de Anglais | MEDLINE | ID: mdl-7844676

RÉSUMÉ

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.


Sujet(s)
Aminoacidopathies congénitales/diagnostic , Kératose palmoplantaire/diagnostic , Lumière/effets indésirables , Tyrosine/sang , Aminoacidopathies congénitales/complications , Aminoacidopathies congénitales/diétothérapie , Enfant d'âge préscolaire , Humains , Kératose palmoplantaire/diétothérapie , Kératose palmoplantaire/étiologie , Mâle
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