Dyskeratosis Congenita Without Oral Involvement: A Rare Hereditary Disease
Dyskeratosis congenita (DC) is a rare, progressive, multi-system, inherited disorder of telomere biology, first described in 1906 as the Zinsser–Engman–Cole syndrome. The condition presents with the classic triad of nail dystrophy, reticulate skin pigmentation, and oral leukoplakia. Variable somatic...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Oman Medical Specialty Board
2015-05-01
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Series: | Oman Medical Journal |
Subjects: | |
Online Access: | http://www.omjournal.org/fultext_PDF.aspx?DetailsID=656&type=fultext |