Further delineation of the 3-M syndrome with review of the literature

Am J Med Genet. 1987 Sep;28(1):195-209. doi: 10.1002/ajmg.1320280127.

Abstract

The 3-M syndrome is a clinically recognizable disorder characterized by prenatal and postnatal growth retardation and a spectrum of consistent minor anomalies. Intelligence seems normal. Inheritance is probably autosomal recessive, with possible expression of the mutant gene in the heterozygote. Three sibs with the 3-M syndrome are reported, together with an extensive review of the pertinent literature.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Bone Diseases, Developmental / diagnostic imaging
  • Bone Diseases, Developmental / genetics*
  • Female
  • Growth Disorders / diagnostic imaging
  • Growth Disorders / genetics*
  • Humans
  • Joint Dislocations / genetics
  • Male
  • Pedigree
  • Radiography
  • Syndrome