Abstract
We report on a boy with unique somatic and skeletal manifestations. The syndrome consists of mental retardation, postaxial polydactyly, phalangeal hypoplasia, 2–3 toe syndactyly, abnormal face and uncombable hair. A younger sib who died soon after the birth was probably also affected. Am. J. Med. Genet. 68:142–146, 1997 © 1997 Wiley-Liss, Inc.
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