Figuera L E, Rivas F, Cantú J M
División de Genética, CMNO-IMSS, Guadalajara, Jalisco, Mexico.
Clin Genet. 1993 Oct;44(4):190-2. doi: 10.1111/j.1399-0004.1993.tb03877.x.
The oral-facial-digital (OFD) syndromes constitute a heterogeneous group of entities usually associated with certain features that permit a specific diagnosis. This report refers to a 10-month-old girl with cleft palate, mesomelic limb shortening, oligopolydactyly, and fibular aplasia. Since this combination has not been described previously, it is proposed as a distinct type of oral-facial-digital syndrome, and we suggest mutations of homeotic genes to explain some abnormalities present in the OFD syndromes.