Search results for "Neurofibromatosis type I"

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Oral manifestations of Type I Neurofibromatosis in a family

2011

Neurofibroma is a benign peripheral nerve sheath tumor. It is one of the most frequent tumors of neural origin and its presence is one of the clinical criteria for the diagnosis of neurofibromatosis type I (NF-I). Neurofibromatosis type I is an autosomal dominantly inherited disease due to an alteration in the long arm of chromosome 17. About 50% of NF-I patients have no family history of the disease. NF-I patients have skin lesions (café au lait spots and neurofibromas) as well as bone malformations and central nervous system tumors. Diagnosis is based on a series of clinical criteria. NF-I presents with certain definite oral manifestations which confers to the dentists a major responsibil…

Neurofibromatosis type IPathologymedicine.medical_specialtybusiness.industryOdontologíaDisease:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludChromosome 17 (human)Café au lait spotUNESCO::CIENCIAS MÉDICASmedicineNeurofibromaFamily historyNeurofibromatosismedicine.symptombusinessGeneral DentistryPeripheral Nerve SheathJournal of Clinical and Experimental Dentistry
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