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Am J Med Genet. 1995 Jul 3;57(3):377-9.

Michels syndrome in a Brazilian girl born to consanguineous parents.

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  • 1Serviço de Genética Clinica, Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Brazil.

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.

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