Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles

Genet Couns. 1999;10(3):265-9.

Abstract

We report two siblings from non consanguineous parents with a similar MCA/MR syndrome: Pre- and postnatal growth retardation, microcephaly, mental retardation, iris colobomata, facial dysmorphism, spasticity, dilated ventricles and abnormal immunoglobulin levels. Review of published reports and the use of the London Dysmorphology Database suggests that these siblings may present a new syndrome.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child, Preschool
  • Craniofacial Abnormalities / genetics*
  • Face / abnormalities*
  • Female
  • Growth Disorders / genetics*
  • Heart Ventricles / abnormalities*
  • Humans
  • Infant
  • Intellectual Disability / genetics*
  • Iris Diseases / genetics*
  • Microcephaly / genetics
  • Muscle Spasticity / genetics*
  • Nuclear Family
  • Syndrome