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

C. Cunniff, K. Lyons Jones

Research output: Contribution to journalArticlepeer-review

11 Scopus citations


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.

Original languageEnglish (US)
Pages (from-to)28-30
Number of pages3
JournalAmerican journal of medical genetics
Issue number1
StatePublished - 1990


  • Michels syndrome
  • autosomal recessive inheritance
  • craniosynostosis
  • lid abnormalities

ASJC Scopus subject areas

  • Genetics(clinical)


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