distal muscular dystrophy
myotonia atrophica
myotonic dystrophy
Steinert's disease
myotonic muscular dystrophy
Becker muscular dystrophy
zaspopathy
pseudohypertrophic dystrophy
Duchenne's muscular dystrophy
limb-girdle muscular dystrophy
myodystrophy
oculopharyngeal muscular dystrophy
dystrophinopathy
dysferlinopathy
myodegeneration
reverse anorexia nervosa
amyoplasia
dystrophy
muscular dystrophy
dystrophin
white muscle disease
dyschondrosteosis
musculodystrophy
titinopathy
arthrogryposis
Lambert-Eaton myasthenic syndrome
campomelia
opsismodysplasia
osteosarcopenia
Baller-Gerold syndrome
sarcospan
movement disorder
sarcopenia
calpainopathy
amyotrophic lateral sclerosis
geniohyoid
cacomelia
osseoaponeurotic
musclesome
shape
limbic
myoarchitecture
facioscapulohumeral
remuscularization
dystrobrevin
musculosity
muscularness
carnify
dystrophia
pleomorphic rhabdosarcoma
McArdle's disease
musclebound
muscledom
fasciomuscular
dolichostenomelia
sarcolysis
chondrodystrophy
musculofascial
pleomorphic rhabdomyosarcoma
dyskinetoplasty
inclusion body myositis
Hurler's disease
osteosclerosis congenita
lipochondrodystrophy
Hurler's syndrome
neomuscularized
osteomuscular
gargoylism
dysostosis multiplex
myobiology
Kocher-Debre-Semelaigne syndrome
achondroplasty
achondroplasia
Léri-Weill dyschondrosteosis
myogenin
mesomorph
myasthenia gravis
pleurothotonus
extensor
muscular structure
asynergy
muscle system
musculoarticular
myasthenia
extensor muscle
dynapenia
rigor mortis
musculature
Dejerine-Sottas disease
dysmetria
dystrophication
facial muscle
Madelung's deformity
retrolimbic
cachexia
fixator

English words for 'a form of muscular dystrophy that sets in between 40 and 60 years of age and is characterized by weakness and wasting of the muscles of the hands and forearms and lower legs; inheritance is autosomal dominant'

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