Telecanthus hypertelorism strabismus pes cavus Orphanet
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.
Type: Reference Material
Author/Contact: Not Available
Submitted by: admin
Added: Thu Oct 25 2007