Further Heterogeneity of the Oral-Facial-Digital Syndromes
- 1 May 1976
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Pediatrics & Adolescent Medicine
- Vol. 130 (5), 548-554
- https://doi.org/10.1001/archpedi.1976.02120060094018
Abstract
• Two patients with polysyndactyly of the halluces and typical features of oral-facial-digital syndrome, type I (OFD I), are described. Previously, bilateral hallucal polysyndactyly was considered to be a distinctive feature of OFD II, Mohr syndrome. The original classification of OFD II was based on clinical similarities between the affected members of the Mohr-Claussen kindred and the two siblings described by Rimoin and Edgerton. Review of these cases demonstrates important clinical differences, so that justification for the original classification of OFD II is questioned. Retrospectively, a small number of individuals have been considered to have had OFD II, but on review these cases appear to represent a clinically heterogeneous group of disorders. (Am J Dis Child 130:548-554, 1976)This publication has 7 references indexed in Scilit:
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