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Amyotrophie spinale
Amyotrophie spinale avec détresse respiratoire type 1
Amyotrophie spinale avec détresse respiratoire type 2
Amyotrophie spinale diaphragmatique type 2
Côlon irritable
Diarrhée
Distale
Dyspepsie
Dysurie
Fazio-Londe
Flatulence
Forme scapulo-péronière
Gastrique
Hoquet
Hyperventilation
Kugelberg-Welander
Mictions fréquentes
Névrose cardiaque
Paralysie bulbaire progressive de l'enfant
Spasme du pylore
Syndrome de Da Costa
Toux
Werdnig-Hoffman

Translation of "Amyotrophie spinale avec détresse respiratoire type 1 " (French → English) :

TERMINOLOGY
see also In-Context Translations below
amyotrophie spinale avec détresse respiratoire type 1

Autosomal recessive distal spinal muscular atrophy 1
SNOMEDCT-BE (disorder) / 711483003
SNOMEDCT-BE (disorder) / 711483003


amyotrophie spinale avec détresse respiratoire type 2

Diaphragmatic spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 770727008
SNOMEDCT-BE (disorder) / 770727008


Amyotrophie spinale (de):adulte | distale | enfant, type II | forme juvénile, type III [Kugelberg-Welander] | forme scapulo-péronière | Paralysie bulbaire progressive de l'enfant [Fazio-Londe]

Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form
WORLD HEALTH ORGANIZATION ICD-10: G12.1
WORLD HEALTH ORGANIZATION ICD-10: G12.1


amyotrophie spinale distale autosomique récessive type 2

Distal hereditary motor neuropathy Jerash type
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003


amyotrophie spinale diaphragmatique type 2

A rare genetic motor neuron disease with characteristics of progressive early respiratory failure associated with diaphragm paralysis, distal muscular weakness, joint contractures, and axial hypotonia with preserved antigravity limb movements. The ph
SNOMEDCT-BE (disorder) / 770727008
SNOMEDCT-BE (disorder) / 770727008


Amyotrophie spinale infantile, type I [Werdnig-Hoffman]

Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
WORLD HEALTH ORGANIZATION ICD-10: G12.0
WORLD HEALTH ORGANIZATION ICD-10: G12.0


Définition: Le patient attribue ses symptômes au trouble somatique d'un système ou d'un organe innervé et contrôlé, en grande partie ou entièrement, par le système neurovégétatif: système cardio-vasculaire, gastro-intestinal, respiratoire, et urogénital. Les symptômes sont habituellement de deux types, aucun des deux n'évoquant un trouble somatique de l'organe ou du système concerné. Le premier type concerne des plaintes en rapport avec des signes objectif ...[+++]

Definition: Symptoms are presented by the patient as if they were due to a physical disorder of a system or organ that is largely or completely under autonomic innervation and control, i.e. the cardiovascular, gastrointestinal, respiratory and urogenital systems. The symptoms are usually of two types, neither of which indicates a physical disorder of the organ or system concerned. First, there are complaints based upon objective signs of autonomic arousal, such as palpitations, sweating, flushing, tremor, and expression of ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F45.3
WORLD HEALTH ORGANIZATION ICD-10: F45.3
IN-CONTEXT TRANSLATIONS


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Amyotrophie spinale avec détresse respiratoire type 1

Date index:2022-08-16 -

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