RT - Journal Article T1 - A case report of neurofibromatosis JF - Caspian-J-Dent-Res YR - 2014 JO - Caspian-J-Dent-Res VO - 3 IS - 1 UR - http://cjdr.ir/article-1-104-en.html SP - 47 EP - 51 K1 - Neurofibromatosis type I K1 - Neuorofibroma K1 - Cutanous neuorofibroma K1 - Hard palate AB - Introduction:Neurofibromatosis is a genetic disease characterized by multifocal benign tumors of peripheral nerves, called neurofibromas, and pigmented spots on the skin which inherited as autosomal-dominant. The most common form of the disease is neurofibromatosis type 1, also known as von Recklinghausen's disease of the skin. When an individual has small number of lesions in a limited region of the his body, it could be missed by the patient or not acknowledged by the clinicians as a form of neurofibromatosis.We present here, a case of an 18-year-old male with neurofibromatosis type 1who referred to Babol Dental School for a routine dental examination. LA eng UL http://cjdr.ir/article-1-104-en.html M3 10.22088/cjdr.3.1.47 ER -