MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS
| Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
|---|---|
| Data(s) |
20/05/2014
20/05/2014
03/07/1995
|
| Resumo |
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. |
| Formato |
377-379 |
| Identificador |
http://dx.doi.org/10.1002/ajmg.1320570302 American Journal of Medical Genetics. New York: Wiley-liss, v. 57, n. 3, p. 377-379, 1995. 0148-7299 http://hdl.handle.net/11449/35532 10.1002/ajmg.1320570302 WOS:A1995RF08300001 |
| Idioma(s) |
eng |
| Publicador |
Wiley-Blackwell |
| Relação |
American Journal of Medical Genetics |
| Direitos |
closedAccess |
| Palavras-Chave | #CRANIOSYNOSTOSIS #EYELID ABNORMALITIES #HYPERTELORISM #CLEFTING #MICHELS SYNDROME |
| Tipo |
info:eu-repo/semantics/article |
