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Dyskeratosis congenita : report of a case with literature review

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Dyskeratosis congenita : report of a case with literature review

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dc.contributor.author Auluck, Ajit es
dc.date.accessioned 2017-11-21T10:51:22Z
dc.date.available 2017-11-21T10:51:22Z
dc.date.issued 2007 es
dc.identifier.citation Auluck, Ajit. Dyskeratosis congenita : report of a case with literature review. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 12 5 2007: 8- es
dc.identifier.uri http://hdl.handle.net/10550/63192
dc.description.abstract Leukoplakic lesion is not uncommon in clinical practice but its occurrence as a component of a syndrome is rare. Dyskeratosis congenita is a rare genodermatosis, which is characterized by triad of skin pigmentation, nail dystrophy and leukoplakic lesion in the oral cavity. It is important for dentists to now about Dyskeratosis Congenita because these leukoplakic lesions can spontaneously undergo malignant transformation. Majority of cases have been reported in dermatology or pediatrics literature whereas only few reports have appeared in dental literature. The purpose of reporting this case with review of recent literature is to create better awareness among dentists about the multisystem manifestations and oro-dental abnormalities of this fatal condition that can aid clinicians in early diagnosis. A case of 26 year old male is reported with details of differential diagnosis, importance of hematological investigations, periodic biopsies and current concepts in management of such patients are briefly reviewed. es
dc.title Dyskeratosis congenita : report of a case with literature review es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.identifier.doi es
dc.type.hasVersion VoR es_ES

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