Orofaciodigital syndrome X

Oral-facial-digital syndrome, type 10 is characterized by facial (telecanthus, flat nasal bridge, retrognathia), oral (cleft palate, vestibular frenula) and digital (oligodactyly, preaxial polydactyly) features, associated with remarkable radial shortening, fibular agenesis and coalescence of tarsal bones. The syndrome has been described in one 10-month-old girl. No new cases have been described since 1993.

Also known as: Figuera syndrome, OFD10, oral-facial-digital syndrome type 10, orofaciodigital syndrome X, orofaciodigital syndrome type 10, orofaciodigital syndrome type X, orofaciodigital syndrome with fibular aplasia, OFD syndrome 10

0 clinical trials for this condition and its sub-types, 0 tagged with Orofaciodigital syndrome X itself.