Telecanthus-hypertelorism-strabismus-pes cavus syndrome

MONDO:0017997

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

0 clinical trials for this condition and its sub-types, 0 tagged with Telecanthus-hypertelorism-strabismus-pes cavus syndrome itself.

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↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59)

Including sub-types (0) Tagged with Telecanthus-hypertelorism-strabismus-pes cavus syndrome (0)

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