Autosomal dominant inheritance of Brachmann-de Lange syndrome

Am J Med Genet. 1996 Dec 30;66(4):445-8. doi: 10.1002/(SICI)1096-8628(19961230)66:4<445::AID-AJMG12>3.0.CO;2-U.

Abstract

A mother with mild phenotype and her severely affected son, both with classic manifestations of Brachmann-de Lange syndrome (BDLS), are described. This documented mother-to-child transmission supports the hypothesis of autosomal dominant transmission with intrafamilial variability. Known cases of BDLS with autosomal dominant inheritance are reviewed. Although most cases of BDLS are sporadic, a careful evaluation of parents of affected children is important for appropriate genetic counseling.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • De Lange Syndrome / diagnosis
  • De Lange Syndrome / genetics*
  • Female
  • Genes, Dominant*
  • Humans
  • Infant
  • Male
  • Pedigree