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Becker
Benign
Benign scapuloperoneal with early contractures
CMD
Congenital muscular dystrophy
Congenital muscular dystrophy NOS
Congenital muscular dystrophy type 1B
Congenital muscular dystrophy type 1B
DMD
Disease central core
Distal
Duchenne
Duchenne disease
Duchenne dystrophy
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Duchenne-Griesinger disease
Emery-Dreifuss
Erb atrophy
Erb dystrophy
FCMD
Facioscapulohumeral
Fukuyama-type congenital muscular dystrophy
Limb-girdle
Meryon's disease
Minicore
Multicore
Muscular dystrophy - Duchenne type
Nemaline
Ocular
Oculopharyngeal
Pseudohypertrophic muscular dystrophy
Salih congenital muscular dystrophy
Scapuloperoneal
Severe
Zimmerlin atrophy

Translation of "fukuyama-type congenital muscular dystrophy " (English → French) :

Fukuyama-type congenital muscular dystrophy | FCMD [Abbr.]

dystrophie musculaire congénitale de Fukuyama
IATE - Health
IATE - Health


congenital muscular dystrophy | CMD [Abbr.]

dystrophie musculaire congénitale | DMC [Abbr.]
IATE - Health
IATE - Health


Congenital muscular dystrophy type 1B

dystrophie musculaire congénitale type 1B
SNOMEDCT-BE (disorder) / 764944006
SNOMEDCT-BE (disorder) / 764944006


Congenital muscular dystrophy type 1B (disorder)

CMD1B - congenital muscular dystrophy type 1B
SNOMEDCT-BE (disorder) / 764944006
SNOMEDCT-BE (disorder) / 764944006


Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline

Disproportion des types de fibres Dystrophie musculaire congénitale:SAI | avec anomalies morphologiques spécifiques des fibres musculaires | Myopathie:à axe central | à bâtonnets [némaline] | de type: mini-core | multi-core | myotubulaire (centro-nucléaire)
WORLD HEALTH ORGANIZATION ICD-10: G71.2
WORLD HEALTH ORGANIZATION ICD-10: G71.2


Salih congenital muscular dystrophy

myopathie précoce avec cardiomyopathie létale
SNOMEDCT-BE (disorder) / 702343002
SNOMEDCT-BE (disorder) / 702343002


Duchenne muscular dystrophy | Duchenne type muscular dystrophy | Duchenne's muscular dystrophy | Meryon's disease | Muscular dystrophy - Duchenne type | pseudohypertrophic muscular dystrophy | DMD [Abbr.]

dystrophie musculaire de Duchenne | myopathie de Duchenne | myopathie primitive progressive pseudo-hypertrophique type Duchenne-Griesinger | myopathie pseudo-hypertrophique de Duchenne | DMD [Abbr.]
IATE - Health
IATE - Health


Duchenne muscular dystrophy [ Duchenne type muscular dystrophy | Duchenne dystrophy | Duchenne disease | Erb dystrophy | Duchenne-Griesinger disease | Zimmerlin atrophy | Erb atrophy ]

maladie de Duchenne de Boulogne
Muscles and Tendons | Symptoms (Medicine)
Muscles et tendons | Symptômes (Médecine)


Muscular dystrophy:autosomal recessive, childhood type, resembling Duchenne or Becker | benign [Becker] | benign scapuloperoneal with early contractures [Emery-Dreifuss] | distal | facioscapulohumeral | limb-girdle | ocular | oculopharyngeal | scapuloperoneal | severe [Duchenne]

Dystrophie musculaire:autosomique récessive, infantile, de type Duchenne ou Becker | bénigne [Becker] | des ceintures | distale | facio-scapulo-humérale | oculaire | oculo-pharyngée | scapulo-péronière:SAI | bénigne avec contractures précoces [Emery-Dreifuss] | sévère [Duchenne]
WORLD HEALTH ORGANIZATION ICD-10: G71.0
WORLD HEALTH ORGANIZATION ICD-10: G71.0




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'fukuyama-type congenital muscular dystrophy'

Date index:2023-06-30 -

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