Telecanthus hypertelorism strabismus pes cavus Orphanet

Description: Summary This syndrome is characterized by telecanthus, hypertelorism, strabismus, pes cavus and variable anomalies. It has been described in a father and his son. The latter also had hypospadias, bilateral inguinal hernia, clinodactyly and camptodactyly of fingers, and radiographic findings including flared metaphyses of long bones and osteopenia.