A case report of neurofibromatosis

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 Reckling...

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Главные авторы: Shimae Nafarzadeh (Автор), Mina Motallebnejad (Автор), Anahita Ghorbani (Автор), Naghmeh Jamaatlou (Автор)
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Опубликовано: Babol University of Medical Sciences, 2014-03-01T00:00:00Z.
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Итог: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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2322-2395