TWO CASES OF TYROSINEMIA TYPE II, AND ITS RARE OCCURRENCE IN TWO BROTHERS

Authors

  • A BAGHERI
  • B EINOLLAHI
  • MA JAVADI From the Department of Ophthalmology, Labbafinejad Medical Center, Shahid Beheshti University of Medical Sciences, Tehran
  • SA MIRDEHGHAN
  • Y DOWLATI the Center for Research and Education in Skin Disease and Leprosy, p.o. Box 14155-6383, Tehran, Islamic Republic of Iran
Abstract:

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.

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two cases of tyrosinemia type ii, and its rare occurrence in two brothers

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Journal title

volume 10  issue 2

pages  169- 173

publication date 1996-08

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