معرفی یک بیمار مبتلا به مارگزیدگی با گانگرن انگشتان دست ها و پاها

Authors

  • عارفی, سید حسن
  • کمال هدایت, داریوش
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معرفی یک بیمار مبتلا به سندرم ایکتیوزلاملار

Introduction: Ichthyosis lamellar syndrome is a rare genodermatosis and in most families is inherited as an autosomal recessive trait because of transglutaminase-1 deficiency. Case Report: Our patient was a 6 year old girl and she was the result of consanguinity. She had large plate-like scales. The scales had mosaic-like pattern and erythroderma was absent. Tautness of her facial skin was as...

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Journal title

volume 39  issue None

pages  11- 13

publication date 1986-03

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