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bn:00029006n
Noun Concept
SYL
No term available
EN
The most common form of muscular dystrophy; inheritance is X-linked recessive (carried by females but affecting only males) WordNet 3.0
Relations
Sources
IS A
EN
muscular dystrophy
EN
rare disease
DRUG USED FOR TREATMENT
EN
Ataluren
EN
deflazacort
EN
eteplirsen
GENETIC ASSOCIATION
EN
dystrophin
HAS CAUSE
EN
mutation
HEALTH SPECIALTY
EN
neurology
MEDICAL EXAMINATIONS
EN
electromyography
EN
genetic screening
EN
magnetic resonance imaging
EN
muscle biopsy
EN
sleep study
NAMED AFTER
EN
Guillaume Duchenne de Boulogne
POSSIBLE TREATMENT
EN
corticosteroid
EN
artificial respiration
EN
occupational therapy
EN
physical therapy
EN
surgery
+1 relations
SYMPTOMS
EN
amyotrophia
EN
cardiomyopathy
EN
myasthenia

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