Böök syndrome

Book syndrome is a rare autosomal dominant ectodermal dysplasia syndrome reported in a Swedish family (25 cases from 4 generations), and one isolated case, and is characterized by premolar aplasia, hyperhidrosis, and premature graying of the hair. Additional features reported in the isolated case include a narrow palate, hypoplastic nails, eyebrow anomalies, a unilateral simian crease, and poorly formed dermatoglyphics.

Also known as: Böök syndrome, book syndrome, PHC syndrome, premolar aplasia, hyperhidrosis, and canities prematura

0 clinical trials for this condition and its sub-types, 0 tagged with Böök syndrome itself.