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Up to: Hereditary neoplastic syndrome · Ectodermal dysplasia syndrome

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.

12 trials tagged with this condition →

DKC1-related disorder 0 trials · 3 incl. sub-types Sub-types →
Revesz syndrome 2 trials
Dyskeratosis congenita and related telomere biology disorder 1 trial Sub-types →
Autosomal recessive dyskeratosis congenita 4 0 trials
Dyskeratosis congenita, autosomal dominant 1 0 trials
Dyskeratosis congenita, autosomal dominant 2 0 trials
Dyskeratosis congenita, autosomal dominant 3 0 trials
Dyskeratosis congenita, autosomal dominant 4 0 trials
Dyskeratosis congenita, autosomal dominant 6 0 trials
Dyskeratosis congenita, autosomal recessive 1 0 trials
Dyskeratosis congenita, autosomal recessive 2 0 trials
Dyskeratosis congenita, autosomal recessive 3 0 trials
Dyskeratosis congenita, autosomal recessive 6 0 trials
Dyskeratosis congenita, autosomal recessive 7 0 trials
Dyskeratosis congenita, autosomal recessive 8 0 trials
Dyskeratosis congenita, digenic 0 trials