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
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Case Reports
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Abnormalities, Multiple / genetics*
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Child, Preschool
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Craniosynostoses / complications
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Craniosynostoses / genetics*
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Eyelids / abnormalities*
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Female
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Genes, Recessive
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Humans
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Intellectual Disability / complications
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Intellectual Disability / genetics
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Syndrome