Resources > OCOSH Classification > Foot Deformities > Acquired Foot Deformities > Pes Cavus > Telecanthus hypertelorism strabismus pes cavus Orphanet
PreviousTelecanthus hypertelorism strabismus pes cavus Orphanet (Visit this link)
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.
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Added: Thu Oct 25 2007
