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Aran-Duchenne disease
Basedow disease
Basedow's disease
Basedow's syndrome
Becker
Begbie's disease
Benign
Benign scapuloperoneal with early contractures
Cruveilhier disease
DMD
Diffuse toxic goiter
Disease
Distal
Duchenne
Duchenne disease
Duchenne dystrophy
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Duchenne-Erb syndrome
Duchenne-Griesinger disease
Emery-Dreifuss
Erb atrophy
Erb dystrophy
Erb's palsy
Erb-Duchenne palsy
Erb-Duchenne paralysis
Exophthalmic goiter
Facioscapulohumeral
Flajani's disease
Flajani-Basedow syndrome
Graves disease
Graves' disease
Haemoglobinuria
Haemolytic anaemia cold type
Human disease
Illness
Limb-girdle
Marsh's disease
Meryon's disease
Muscular dystrophy - Duchenne type
Ocular
Oculopharyngeal
PMA
Parry's disease
Progressive muscular atrophy
Progressive spinal muscular atrophy
Pseudohypertrophic muscular dystrophy
SMA
SPMA
Scapuloperoneal
Severe
Spinal muscular atrophy
Spinal progressive muscular atrophy
Struma exophthalmica
Upper brachial plexus paralysis
Von Basedow disease
Warm type
Zimmerlin atrophy

Translation of "duchenne disease " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]

amyotrophie d'Aran-Duchenne | amyotrophie spinale progressive | atrophie de Cruveilhier | atrophie musculaire progressive d'Aran | maladie d'Aran-Duchenne
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)


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-Erb syndrome | Erb-Duchenne paralysis | upper brachial plexus paralysis

atteinte du plexus brachial inférieur | paralysie d'Erb-Duchenne | syndrome de Déjerine-Klumpke | syndrome radiculaire supérieur du plexus brachial
IATE - Health
IATE - Health


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


illness [ disease | human disease(GEMET) ]

maladie [ affection ]
28 SOCIAL QUESTIONS | MT 2841 health | NT1 allergy | NT1 blood disease | NT1 cancer | NT1 cardiovascular disease | NT1 chronic illness | NT1 congenital disease | NT1 disease of the nervous system | NT1 endemic disease | NT1 endocrine disease |
28 QUESTIONS SOCIALES | MT 2841 santé | NT1 allergie | NT1 cancer | NT1 épidémie | NT1 maladie cardio-vasculaire | NT1 maladie chronique | NT1 maladie congénitale | NT1 maladie d'origine alimentaire | NT1 maladie de la nutrition | NT2 malnutriti


Erb's palsy [ Erb-Duchenne palsy ]

paralysie radiculaire supérieure [ paralysie de Duchenne-Erb ]
Nervous System
Système nerveux


Graves' disease [ Graves disease | Basedow's disease | Basedow disease | von Basedow disease | Basedow's syndrome | exophthalmic goiter | diffuse toxic goiter | struma exophthalmica | Flajani's disease | Flajani-Basedow syndrome | Parry's disease | Marsh's disease | Begbie's disease ]

maladie de Basedow [ maladie de Graves | goitre exophtalmique | maladie de Parry | maladie de Flajani ]
Hypophysis | Human Diseases - Various
Hypophyse | Maladies humaines diverses


Autoimmune haemolytic disease (cold type)(warm type) Chronic cold haemagglutinin disease Cold agglutinin:disease | haemoglobinuria | Haemolytic anaemia:cold type (secondary)(symptomatic) | warm type (secondary)(symptomatic)

Anémie hémolytique:type chaud (secondaire) (symptomatique) | type froid (secondaire) (symptomatique) | Hémoglobinurie à agglutinines froides Maladie (à):agglutinines froides | chronique à hémagglutinines froides | hémolytique auto-immune (type chaud) (type froid)
WORLD HEALTH ORGANIZATION ICD-10: D59.1
WORLD HEALTH ORGANIZATION ICD-10: D59.1


Enteroviral lymphonodular pharyngitis Foot-and-mouth disease Tanapox virus disease Yaba pox virus disease

Fièvre (de):aphteuse | Yaba | Pharyngite lymphonodulaire à entérovirus Syndrome du virus de Tanapox
WORLD HEALTH ORGANIZATION ICD-10: B08.8
WORLD HEALTH ORGANIZATION ICD-10: B08.8
IN-CONTEXT TRANSLATIONS
Parents may have a high risk of transmitting severe life-threatening disorders, such as Duchenne muscular dystrophy, cystic fibrosis, Tay-Sachs disease, and many other similar conditions.

Des parents peuvent présenter un risque élevé de transmission de maladies graves et mortels, comme la dystrophie musculaire Duchenne, la fibrose kystique, la maladie de Tay-Sachs, et de nombreuses autres conditions semblables.


Some well known rare diseases are Cystic fibrosis, Haemophilia and Duchenne muscular dystrophy.

Parmi les maladies rares les plus connues, citons la fibrose cystique, l’hémophilie et la dystrophie musculaire de Duchenne.


An example of a disease in this category is Duchenne muscular dystrophy.

Un exemple de ce type de maladie est la dystrophie musculaire de Duchenne.




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'duchenne disease'

Date index:2022-10-25 -

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