علیان, زهرا

[ 1 ] - سندرم ریخنر هانارت (تیروزینمی تیپ 2) یک گزارش موردی از تاخیر تشخیص با ضایعات هایپرکراتوتیک دست و پا

Introduction: Richner-Hanhart syndrome (tyrosinemia type II) is a rare autosomal recessive disease associated with high serum tyrosine levels caused by the deficiency of tyrosine ami-notransferase enzyme. Case Report: We report a 7-year-old female patient with complaints of hyperkeratosis lesions of palms and soles which started 3 years ago. Chromatography of serum amino acids showed a tyrosine...