Dyskeratosis congenita: a case report and review of literature

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Dyskeratosis congenita: a case report and review of literature

Dyskeratosis congenita (DC) is classically characterised by a mucocutaneous triad of reticulated poikiloderma, nail dystrophy and mucosal leukoplakia together with bone marrow failure and increased risk of malignancy1- 4. Due to its rarity and clinical heterogeneity it is not easily recognised and p...

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Bibliographic Details
Main Authors:	Shamsudin, Norashikin, Kader Ibrahim, Sabeera Begum
Format:	Article
Language:	English
Published:	Persatuan Dermatologi Malaysia 2014
Online Access:	http://psasir.upm.edu.my/id/eprint/37178/ http://psasir.upm.edu.my/id/eprint/37178/1/Dyskeratosis%20congenita.pdf

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