TY - JOUR T1 - Orofaciodigital syndrome with mesomelic limb shortening. JF - Journal of Medical Genetics JO - J Med Genet SP - 189 LP - 192 DO - 10.1136/jmg.21.3.189 VL - 21 IS - 3 AU - J Burn AU - C Dezateux AU - C M Hall AU - M Baraitser Y1 - 1984/06/01 UR - http://jmg.bmj.com/content/21/3/189.abstract N2 - Two sisters, the children of first cousin Pakistani Moslem parents, have unusual facies, tongue hamartomata, pre- and postaxial polydactyly, severe talipes, and mesomelic limb shortening associated with tibial dysplasia. Homozygosity for a recessive gene defect is probable. The phenotype resembles, but is distinct from, the orofaciodigital syndromes delineated to date. We suggest that this condition be labelled OFD IV. ER -