Dyskeratosis Congenita: A Rare Case.
Article
in English
| IMSEAR
| ID: sea-177196
ABSTRACT
Dyskeratosis congenita (DKC) is a rare genodermatosis which exhibits oral leukoplakia, nail dystrophy, and reticular skin pigmentations as its primary features. Dyskeratosis congenita has increased risk of developing constitutional anemia and malignancies and early diagnosis enables the patient to be monitored and proper interventional therapy to be instituted. Here, we present an interesting and rare case report of DKC. Very few are being reported in our country and we, as physicians, should be aware of DKC, presenting as pyrexia, and anemia.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Type of study:
Screening study
Language:
English
Year:
2016
Type:
Article
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