MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS

Guionalmeida, M. L.; Rodini, ESO

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/35532

Title:

MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS

Author(s):

Institution:

Universidade Estadual Paulista (UNESP)

ISSN:

0148-7299

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.

Issue Date:

3-Jul-1995

Citation:

American Journal of Medical Genetics. New York: Wiley-liss, v. 57, n. 3, p. 377-379, 1995.

Time Duration:

377-379

Publisher:

Wiley-Blackwell

Keywords:

CRANIOSYNOSTOSIS
EYELID ABNORMALITIES
HYPERTELORISM
CLEFTING
MICHELS SYNDROME

Source:

http://dx.doi.org/10.1002/ajmg.1320570302

URI:

Access Rights:

Acesso restrito

Type:

outro

Source:

http://repositorio.unesp.br/handle/11449/35532

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