Craniosynostosis and lid anomalies: report of a girl with Michels syndrome

Am J Med Genet. 1990 Sep;37(1):28-30. doi: 10.1002/ajmg.1320370108.

Abstract

We report on a 2-year-old girl with Michels syndrome, a condition characterized by mental deficiency, craniosynostosis, blepharophimosis, ptosis, and epicanthus inversus. The phenotypic findings are compared with those of previously reported cases.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child, Preschool
  • Craniosynostoses / complications
  • Craniosynostoses / genetics*
  • Eyelids / abnormalities*
  • Female
  • Genes, Recessive
  • Humans
  • Intellectual Disability / complications
  • Intellectual Disability / genetics
  • Syndrome