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Medical Definition of Dyskeratosis congenita
1. An x-linked syndrome occurring predominantly in males, with onset in childhood and characterised by nail dystrophy, reticular cutaneous hyperpigmentation, mucosal leukokeratosis, and pancytopenia resembling that of fanconi. It is also known as zinsser-cole-engman syndrome. (12 Dec 1998)
Lexicographical Neighbors of Dyskeratosis Congenita
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