A Family of Oculopharyngeal Muscular Dystrophy and it's HLA Typing
Journal of the Korean Neurological Association
; : 266-272, 1986.
Article
en Ko
| WPRIM
| ID: wpr-75027
Biblioteca responsable:
WPRO
ABSTRACT
The authors presented a family whose 4 siblings had been suffered from oculopharyngeal muscular dystrophy of autoscmal recessive trend, with symptoms of progressive ptosis, external ophthalmoplegia, dysarthria, dysphagia and facial muscle atrophy, and we performed HLA study on these 9 family members which showed no interrelationship between oculopharyngeal muscular dystrophy and HLA Haplotypes.
Texto completo:
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Índice:
WPRIM
Asunto principal:
Atrofia
/
Haplotipos
/
Prueba de Histocompatibilidad
/
Trastornos de Deglución
/
Oftalmoplejía
/
Distrofia Muscular Oculofaríngea
/
Hermanos
/
Disartria
/
Músculos Faciales
Límite:
Humans
Idioma:
Ko
Revista:
Journal of the Korean Neurological Association
Año:
1986
Tipo del documento:
Article