Kozlowski K, Krajewska M
Department of Radiology, Royal Alexandra Hospital for Children, Sydney, Australia.
Am J Med Genet. 1997 Jan 20;68(2):142-6.
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.