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