Halal F, Silver K
Division of Medical Genetics, Montreal Children's Hospital, McGill University, Quebec, Canada.
Am J Med Genet. 1992 Feb 1;42(3):381-6. doi: 10.1002/ajmg.1320420328.
We report on 4 individuals (3 sibs and their father) with a syndrome of growth retardation, microcephaly, minor facial anomalies reminiscent of a mild Brachmann-de Lange syndrome (BDLS), severe metatarsus adductus, developmental delay, and unusual dermatoglyphics. The syndrome, which seems to be inherited as an autosomal dominant trait with variable expressivity, resembles mild BDLS.