Clouston Syndrome is a rare autosomal dominant disorder cahracterized by hypotrichosis and nail dystrophy along with palmoplantar keratoderma.
Mutations in the GJB6 gene have been shown to be causal for this condition.
Congenital malformations, deformations and chromosomal abnormalities
Other congenital malformations
Autosomal dominant
13q12.11
Clouston Syndrome is a rare autosomal dominant disorder cahracterized by hypotrichosis and nail dystrophy along with palmoplantar keratoderma.
Mutations in the GJB6 gene have been shown to be causal for this condition.