Orofaciodigital syndrome 10
Other Names: OFD10; Oral-facial-digital syndrome 10; OFD syndrome 10; Orofaciodigital syndrome type Figuera; OFDS 10; Orofaciodigital syndrome with fibular aplasia; Oral-facial-digital syndrome with fibular aplasia; Orofaciodigital syndrome X; Oral facial digital syndrome 10; Oral facial digital syndrome type 10
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.
NIH genetic and rare disease info[edit source]
Orofaciodigital syndrome 10 is a rare disease.
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