Dyskeratosis Congenita: A Report of Two Cases
Author(s) -
Anila Karunakaran,
Rathy Ravindran,
Mohammed Asif Arshad,
Mr. K. Sri Ram,
M. K. Shruthi Laxmi
Publication year - 2013
Publication title -
case reports in dentistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.221
H-Index - 11
eISSN - 2090-6447
pISSN - 2090-6455
DOI - 10.1155/2013/845125
Subject(s) - genodermatosis , dyskeratosis congenita , medicine , dermatology , leukoplakia , pediatrics , cancer , dna , biochemistry , chemistry , genetics , telomere , biology , gene
Oral manifestations play an important role in the diagnosis of many systemic conditions. Dyskeratosis congenita (DC) is a rare genodermatosis which exhibits oral leukoplakia, nail dystrophy, and reticular skin pigmentations as its primary features. DC has increased risk of developing constitutional anemias and malignancies and early diagnosis enables the patient to be monitored and proper interventional therapy to be instituted. Hence, dentists need to be aware of the various manifestations of this fatal syndrome. Only few cases have been reported on DC in the dental literature. Two cases of DC are reported here with a brief review of the literature.
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