Guionalmeida, M. L.Rodini, ESO2014-05-202014-05-201995-07-03American Journal of Medical Genetics. New York: Wiley-liss, v. 57, n. 3, p. 377-379, 1995.0148-7299http://hdl.handle.net/11449/35532We 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.377-379engCRANIOSYNOSTOSISEYELID ABNORMALITIESHYPERTELORISMCLEFTINGMICHELS SYNDROMEArtigo10.1002/ajmg.1320570302WOS:A1995RF08300001Acesso restrito