A case report of neurofibromatosis

نویسندگان

  • Anahita Ghorbani ,Department of Oral Medicine, Faculty of Dentistry, Babol University of Medical Sciences, Babol-Iran.
  • Mina Motallebnejad ,Cellular& Molecular Biology Research Center, Department of Oral Medicine, Faculty of Dentistry, Babol University of Medical Sciences, Babol-Iran.
  • Naghmeh Jamaatlou ,Department of Oral & Maxillofacial Pathology, Faculty of Dentistry, Babol University of Medical Sciences, Babol-Iran.
  • Shimae Nafarzadeh ,Department of Oral & Maxillofacial Pathology, Faculty of Dentistry, Babol University of Medical Sciences, Babol-Iran.
چکیده مقاله:

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.

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عنوان ژورنال

دوره 3  شماره None

صفحات  47- 51

تاریخ انتشار 2014-03

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