Two cases of tyrosinemia type II and its rare occurrence in two brothers

ABSTRACT

Tyrosinemia type II is a rare autosomal recessive disorder which 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 low protein diet and a special regimen