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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 |