Caspian journal of dental research (Mar 2014)

A case report of neurofibromatosis

  • Shimae Nafarzadeh,
  • Mina Motallebnejad,
  • Anahita Ghorbani,
  • Naghmeh Jamaatlou

Journal volume & issue
Vol. 3, no. 1
pp. 47 – 51

Abstract

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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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