Two sisters with Toriello-Carey syndrome

Am J Med Genet. 1999 Nov 26;87(3):262-4. doi: 10.1002/(sici)1096-8628(19991126)87:3<262::aid-ajmg13>3.0.co;2-3.

Abstract

Toriello-Carey syndrome comprises agenesis of the corpus callosum, telecanthus, short palpebral fissures, small nose with anteverted nares, Robin sequence, abnormally shaped ears, cardiac defect, and hypotonia. We describe two Japanese sisters with a Toriello-Carey syndrome whose phenotypes were as severe as reported male cases. The younger sister died suddenly at age 4 months. Our patients with a severe phenotype and possible parental consanguinity suggest autosomal recessive inheritance of Toriello-Carey syndrome.

Publication types

  • Case Reports
  • Comment

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Agenesis of Corpus Callosum*
  • Consanguinity
  • Ductus Arteriosus, Patent / genetics
  • Face / abnormalities*
  • Fatal Outcome
  • Female
  • Humans
  • Infant, Newborn
  • Intellectual Disability / genetics*
  • Syndrome
  • Tetralogy of Fallot / genetics*