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Zinsser-Cole-Engmann syndrome: a rare case report with literature review

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Zinsser-Cole-Engmann syndrome: a rare case report with literature review

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dc.contributor.author Chalkoo, Altaf Hussain es
dc.contributor.author Kaul, Vibhuti es
dc.contributor.author Wani, Lateef Ahmad es
dc.date.accessioned 2014-09-17T10:57:57Z
dc.date.available 2014-09-17T10:57:57Z
dc.date.issued 2014 es
dc.identifier.citation Chalkoo, Altaf Hussain ; Kaul, Vibhuti ; Wani, Lateef Ahmad. Zinsser-Cole-Engmann syndrome: a rare case report with literature review. En: Journal of Clinical and Experimental Dentistry, 2014, Vol. 6, No. 3: 303-306 es
dc.identifier.uri http://hdl.handle.net/10550/37942
dc.description.abstract Zinsser-Cole-Engmann syndrome, more commonly known as Dyskeratosis Congenita, is a heritable genodermato - sis having an estimated incidence of 1 in 1 million people. It is important for an oral physician to be aware of this condition as oral leukoplakia occurs in this condition as part of a classic triad along with reticulate skin pigmentation and nail dystrophy. Besides these, there may be myriad multisystem involvement as well. These individuals have a high predilection for developing malignancies as well as other grave life-threatening conditions. Timely diagnosis and management of these cases may help improve their morbidity and mortality, for which oral physicians can play a major role in recognizing the cases. This will only be possible when more of such cases are reported in dental literature. Here we present a case report of a 30 year old male patient who reported to our department with all the characteristic features of the triad and a few additional findings concordant to the disease as well. en_US
dc.subject Odontología es
dc.subject Ciencias de la salud es
dc.title Zinsser-Cole-Engmann syndrome: a rare case report with literature review es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.type.hasVersion VoR es_ES

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