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

Christopher M Cunniff, K. Lyons Jones

Research output: Contribution to journalArticle

8 Citations (Scopus)

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.

Original languageEnglish (US)
Pages (from-to)28-30
Number of pages3
JournalAmerican Journal of Medical Genetics
Volume37
Issue number1
DOIs
StatePublished - 1990
Externally publishedYes

Fingerprint

Craniosynostoses
Intellectual Disability
Oculopalatoskeletal syndrome
Blepharophimosis, Ptosis, and Epicanthus Inversus

Keywords

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

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

Craniosynostosis and lid anomalies : Report of a girl with Michels syndrome. / Cunniff, Christopher M; Lyons Jones, K.

In: American Journal of Medical Genetics, Vol. 37, No. 1, 1990, p. 28-30.

Research output: Contribution to journalArticle

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