Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation

Figure 4

Pedigree of the family. The arrow indicates the proband. The proband’s father, progeny, siblings, and the descendants of each were afflicted in an autosomal-dominant pattern, but there was a great variability in the degree of hypotrichosis and nail dystrophy. None of them had palmoplantar hyperkeratosis. Healthy members are indicated by empty symbols. Affected ones are represented by black-filled symbols.