Dyskeratosis Congenita
Dyskeratosis congenita (DC) is a rare ectodermal dysplasia that often presents with the classic triad of nail dysplasia, skin pigmentary changes, and oral leukoplakia associated with a high risk of bone marrow failure (BMF) and cancer.
Also known as
DC; DKC; Hoyeraal-Hreidarsson syndrome; Zinsser Cole Engman syndrome
Includes 20 related subtypes ↓Hide subtypes ↑
- autosomal recessive dyskeratosis congenita 4
- DKC1-related disorder
- dyskeratosis congenita and related telomere biology disorder
- dyskeratosis congenita, autosomal dominant 1
- dyskeratosis congenita, autosomal dominant 2
- dyskeratosis congenita, autosomal dominant 3
- dyskeratosis congenita, autosomal dominant 4
- dyskeratosis congenita, autosomal dominant 6
- dyskeratosis congenita, autosomal recessive 1
- dyskeratosis congenita, autosomal recessive 2
- dyskeratosis congenita, autosomal recessive 3
- dyskeratosis congenita, autosomal recessive 5
- dyskeratosis congenita, autosomal recessive 6
- dyskeratosis congenita, autosomal recessive 7
- dyskeratosis congenita, autosomal recessive 8
- dyskeratosis congenita, digenic
- dyskeratosis congenita, X-linked
- Hoyeraal-Hreidarsson syndrome
- pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3
- Revesz syndrome
