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Acromegalia
Acromegalie
Acromegaly
Acromegaly and pituitary gigantism
Early acromegaly
Haemochromatosis
Hyperthyroidism
Hypothyroidism
Marie's disease
Marie's syndrome
Pseudo-acromegaly
Thyrotoxicosis

Translation of "acromegaly " (English → French) :

TERMINOLOGY
see also In-Context Translations below
acromegaly [ Marie's disease | Marie's syndrome ]

acromégalie
Symptoms (Medicine)
Symptômes (Médecine)


acromegaly | acromegalia | Marie's disease

acromégalie | maladie de Marie
médecine > sémiologie et pathologie | biologie > hormone et neurotransmetteur
médecine > sémiologie et pathologie | biologie > hormone et neurotransmetteur


early acromegaly

acromégalie précoce
IATE - Health
IATE - Health


acromegaly

acromégalie | hyperéosinophilisme hypophysaire | maladie de P. Marie | mégalacrie
IATE - Health
IATE - Health


pseudo-acromegaly

pseudo-acromégalie
IATE - Health
IATE - Health


Acromegaly and pituitary gigantism

Acromégalie et gigantisme
WORLD HEALTH ORGANIZATION ICD-10: E22.0
WORLD HEALTH ORGANIZATION ICD-10: E22.0


acromegalie

gigantisme
médecine > médecine dentaire
médecine > médecine dentaire


Arthropathy associated with acromegaly+ (M14.5*) Overproduction of growth hormone

Arthropathie associée à l'acromégalie+ (M14.5*) Hypersécrétion de l'hormone somatotrope
WORLD HEALTH ORGANIZATION ICD-10: E22.0
WORLD HEALTH ORGANIZATION ICD-10: E22.0


This syndrome is characterized by severe intellectual deficit, acromegaly and hyperactivity. The syndrome has been described in two half-brothers. Dysarthria, aggressive behavior, a characteristic facies (an acromegalic and triangular face with a lon

syndrome de déficience intellectuelle liée à l'X-acromégalie-hyperactivité
SNOMEDCT-BE (an acromegalic and triangular face with a lon / 719826004
SNOMEDCT-BE (disorder) / 719826004


Arthropathy in:acromegaly and pituitary gigantism (E22.0+) | haemochromatosis (E83.1+) | hypothyroidism (E00-E03+) | thyrotoxicosis [hyperthyroidism] (E05.-+) |

Arthropathie au cours de:acromégalie et gigantisme (E22.0+) | hémochromatose (E83.1+) | hypothyroïdie (E00-E03+) | thyréotoxicose [hyperthyroïdie] (E05.-+) |
WORLD HEALTH ORGANIZATION ICD-10: M14.5*
WORLD HEALTH ORGANIZATION ICD-10: M14.5*
IN-CONTEXT TRANSLATIONS
Rare disorders include such conditions as cystic fibrosis, Huntington's disease, legionnaires' disease, muscular dystrophy, thalassemia, MPS, pulmonary hypertension, Fabry disease, Gaucher disease, ALS, commonly known as Lou Gehrig's disease, Waldenstrom's anemia, AIDS, and acromegaly, to name a few.

Beaucoup de Canadiens croient qu'il s'agit là d'un élément inébranlable du système de santé universel du Canada, mais dans le cas des maladies rares, l'universalité n'est pas au rendez-vous. Les maladies rares comprennent, entre autres, la fibrose kystique, la maladie de Huntington, la maladie du légionnaire, la dystrophie musculaire, la thalassémie, la MPS, l'hypertension pulmonaire, la maladie de Fabry, la maladie de Gaucher, la SLA, communément appelée la maladie de Lou Gehrig, l'anémie de Waldenstrom, le sida et l'acromégalie.




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'acromegaly'

Date index:2022-01-06 -

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