| Literature DB >> 8261648 |
L E Figuera1, F Rivas, J M Cantú.
Abstract
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.Entities:
Mesh:
Year: 1993 PMID: 8261648 DOI: 10.1111/j.1399-0004.1993.tb03877.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438