A Family of Oculopharyngeal Muscular Dystrophy and it's HLA Typing
Journal of the Korean Neurological Association
;
: 266-272, 1986.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Atrophy
/
Haplotypes
/
Histocompatibility Testing
/
Deglutition Disorders
/
Ophthalmoplegia
/
Muscular Dystrophy, Oculopharyngeal
/
Siblings
/
Dysarthria
/
Facial Muscles
Limits:
Humans
Language:
Korean
Journal:
Journal of the Korean Neurological Association
Year:
1986
Type:
Article
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