From the Department of Ophthalmology, Labbafinejad Medical Center, Shahid Beheshti University of Medical Sciences, Tehran
Abstract: (3693 Views)
Tyrosinemia type II is a rare autosomal recessive disorder wich can present
itself with recurrent epithelial keratitis, hyperkeratotic skin lesions and mental
retardation.
This article reports the rare occurrence of this disease in both offsprings (two
brothers) of a family (consanguinous'marriage) who were managed with a lowprotein
diet and a special regimen.
Type of Study:
case report |
Subject:
Ophthalmology