MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS
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Undergraduate course
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Wiley-Blackwell
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Article
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Acesso restrito
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Abstract
We report on a Brazilian girl born to consanguineous parents and presenting with craniosynostosis, telecanthus, blepharophimosis, blepharoptosis, epicanthus inversus, cleft lip and palate, skeletal defects, and hearing loss. This combination of anomalies appears to constitute the Michels syndrome. (C) 1995 Wiley-Liss, Inc.
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Keywords
CRANIOSYNOSTOSIS, EYELID ABNORMALITIES, HYPERTELORISM, CLEFTING, MICHELS SYNDROME
Language
English
Citation
American Journal of Medical Genetics. New York: Wiley-liss, v. 57, n. 3, p. 377-379, 1995.
