A Family of Oculopharyngeal Muscular Dystrophy and it's HLA Typing
Journal of the Korean Neurological Association
;
: 266-272, 1986.
Article
Dans Coréen
| WPRIM
| ID: wpr-75027
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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Atrophie
/
Haplotypes
/
Test d'histocompatibilité
/
Troubles de la déglutition
/
Ophtalmoplégie
/
Dystrophie musculaire oculopharyngée
/
Fratrie
/
Dysarthrie
/
Muscles de la face
Limites du sujet:
Humains
langue:
Coréen
Texte intégral:
Journal of the Korean Neurological Association
Année:
1986
Type:
Article
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