Craniosynostosis and lid anomalies: report of a girl with Michels syndrome.
AMERICAN JOURNAL OF MEDICAL GENETICS（1990）
摘要
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.
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