Ml. Guionalmeida et Eso. Rodini, MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS, American journal of medical genetics, 57(3), 1995, pp. 377-379
We report on a Brazilian girl born to consanguineous parents and prese
nting with craniosynostosis, telecanthus, blepharophimosis, blepharopt
osis, 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.