Tel Hashomer camptodactyly syndrome is a very rare syndrome characterized by camptodactyly, muscle hypoplasia and weakness, skeletal anomalies, and facial dysmorphism. Abnormal dermatoglyphics include: facial asymmetry, hypertelorism, broad nasal bridge, long philtrum, and a small mouth. Until 2005, only 20 cases have been reported worldwide.
The pattern of inheritance suggested for Tel Hashomer camptodactyly syndrome is autosomal recessive; its molecular basis is unknown.