Roberts syndrome and SC phocomelia. A single genetic entity

Clin Genet. 1987 Mar;31(3):170-7. doi: 10.1111/j.1399-0004.1987.tb02790.x.

Abstract

A family with three siblings showing different manifestations of Roberts syndrome or SC phocomelia is described. With regard to previously published cases of familial Roberts syndrome and SC phocomelia we conclude that these two syndromes are one and the same genetic entity.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Banding
  • Ectromelia / genetics*
  • Humans
  • Pedigree
  • Syndrome