Orofaciodigital syndrome type IV: Report of a patient
- 1 February 1989
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 32 (2) , 151-154
- https://doi.org/10.1002/ajmg.1320320202
Abstract
We describe a further patient with the orofaciodigital syndrome type IV. The clinical characteristics include lobulated tongue, pseudo‐cleft of lip, pre‐ and postaxial polydactyly of hands and feet, severe talipes equinovarus, mesomelic limb shortness associated with tibial hypoplasia, and severe bilateral deafness. Five similar cases including the present patient are now on record. Autosomal recessive inheritance is likely.Keywords
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