Three Cases of Mobius Syndrome in a Family
Journal of the Korean Neurological Association
;
: 1035-1041, 1996.
Artigo
em Coreano
| WPRIM
| ID: wpr-129343
ABSTRACT
Mobius syndrome is generally considered to be a static disorder of congenital origin, and is manifested as unilateral or bilateral facial weakness and lateral gaze limitation. In most instances the syndrome occurs sporadically, but rarely familial cases have been reported. We report a family of three members with Mobius syndrome; a 7-year-old girl, a 6-year-old boy, and their 29-year-old mother. Each patient revealed facial diplegia, and unilateral or bilateral lateral rectus palsy. Brain MRI scans showed normal and there were no definite brainstem dysfunctions on electrophysiologic studies.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Encéfalo
/
Tronco Encefálico
/
Imageamento por Ressonância Magnética
/
Doenças do Nervo Abducente
/
Síndrome de Möbius
/
Mães
Limite:
Adulto
/
Criança
/
Feminino
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Neurological Association
Ano de publicação:
1996
Tipo de documento:
Artigo
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