Further delineation of the Baller-Gerold syndrome

Am J Med Genet. 1993 Feb 15;45(4):519-24. doi: 10.1002/ajmg.1320450423.

Abstract

Three new patients with the Baller-Gerold syndrome bring the number of reported cases to 20. In addition to craniosynostosis involving various sutures and preaxial reduction defects of variable severity, affected patients may have anal, urogenital, cardiac, central nervous system, and vertebral defects. Autosomal recessive inheritance is supported by the presence of affected sibs and parental consanguinity.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics
  • Abnormalities, Multiple / pathology*
  • Adult
  • Anal Canal / abnormalities
  • Central Nervous System / abnormalities
  • Craniosynostoses / genetics
  • Craniosynostoses / pathology*
  • Female
  • Heart Defects, Congenital / genetics
  • Humans
  • Infant, Newborn
  • Pregnancy
  • Spine / abnormalities
  • Syndrome
  • Thumb / abnormalities
  • Urogenital Abnormalities