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Oral manifestations of Type I Neurofibromatosis in a family

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Oral manifestations of Type I Neurofibromatosis in a family

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dc.contributor.author Khan, Mubeen es
dc.contributor.author Ohri, Neera es
dc.date.accessioned 2016-06-24T12:26:26Z
dc.date.available 2016-06-24T12:26:26Z
dc.date.issued 2011 es
dc.identifier.citation Khan, Mubeen ; Ohri, Neera. Oral manifestations of Type I Neurofibromatosis in a family. En: Journal of Clinical and Experimental Dentistry, 2011, Vol. 3, No. 5: 483-486 es
dc.identifier.uri http://hdl.handle.net/10550/54240
dc.description.abstract 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 responsibility for accurate diagnosis and report of the disease. The paper aims to highlight the role of an oral diagnostician in first recognition of NF-I in a family via manifestations in the oral cavity en_US
dc.subject Odontología es
dc.subject Ciencias de la salud es
dc.title Oral manifestations of Type I Neurofibromatosis in a family es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.type.hasVersion VoR es_ES

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