Hyperphalangy and clinodactyly of the index finger with Pierre Robin anomaly: Catel‐Manzke syndrome. A case report and review of the literature
- 1 June 1982
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 21 (6) , 407-410
- https://doi.org/10.1111/j.1399-0004.1982.tb01395.x
Abstract
Mandibular hypoplasia, glossoptosis, U‐shaped cleft palate (Pierre Robin anomaly), associated with bilateral index finger malformation and congenital heart disease are described in a male, newborn infant. Review of the features of seven previously published patients, in addition to the patient reported here, confirms the existence of a distinct dysmorphogenesis syndrome. Although all of these eight patients have been males, and most were sporadic, the etiology of this rare malformation syndrome is unknown.Keywords
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