Richner-Hanhart Syndrome: A case report of an 11 month old female
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چکیده
منابع مشابه
Richner-Hanhart syndrome (tyrosinemia type II): a case report of delayed diagnosis with pseudodendritic corneal lesion.
Richner-Hanhart syndrome (tyrosinemia type II) is a rare autosomal recessive disease associated with high serum tyrosine levels caused by the deficiency of tyrosine aminotransferase enzyme. We report a 15-year-old female patient with complaints of bilateral photophobia and tearing, which started during the infancy period. Biomicroscopic examination revealed bilateral circular corneal opacities ...
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ژورنال
عنوان ژورنال: Sri Lanka Journal of Child Health
سال: 2013
ISSN: 2386-110X,1391-5452
DOI: 10.4038/sljch.v42i4.6271