اسماعیل حاجی نصرالله,

[ 1 ] - بروز بدخیمی در ضایعات نوروفیبروماتوز در بیمار مبتلا به وون رکلین هاوزن

Neurofibromatosis (Von Recklinghausen syndrome) is an autosomal dominant genetic disease caused by a mutation in the gene expressing neurofibromin. It is characterized by café-au-lait macules, axillary or inguinal freckling, multiple neurofibromas, and developmental delay. Malignant transformation or sarcomatosis may occur in as many as 1.5-15% of patients. Case report: We present a patient wi...