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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
Amyotrophie spinale et syndromes apparentés
Distale
Fazio-Londe
Forme scapulo-péronière
Kugelberg-Welander
Paralysie bulbaire progressive de l'enfant
Werdnig-Hoffman

Translation of "amyotrophie spinale adulte " (French → English) :

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 bénigne congénitale autosomique dominante

Autosomal dominant benign distal spinal muscular atrophy
SNOMEDCT-BE (disorder) / 763067000
SNOMEDCT-BE (disorder) / 763067000


amyotrophie spinale avec détresse respiratoire type 1

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


amyotrophie spinale proximale autosomique dominante de l'enfance

Disease with characteristics of muscle weakness and atrophy in the lower limbs, most severely affecting the quadriceps. The loss of motor neurons leads to atrophy of the muscles in the lower limbs with manifestations including unsteady walk and walki
SNOMEDCT-BE (disorder) / 772129007
SNOMEDCT-BE (disorder) / 772129007


syndrome d'amyotrophie spinale-malformation de Dandy-Walker-cataracte

Syndrome with characteristics of infantile symmetrical distal muscle weakness and atrophy of the lower limbs, bilateral anterior polar cataracts and Dandy-Walker malformation. It has been described in two brothers. No sensorineural or cognitive defic
SNOMEDCT-BE (disorder) / 723612001
SNOMEDCT-BE (disorder) / 723612001


amyotrophie spinale avec détresse respiratoire type 2

Diaphragmatic spinal muscular atrophy type 2
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


Amyotrophie spinale et syndromes apparentés

Spinal muscular atrophy and related syndromes
WORLD HEALTH ORGANIZATION ICD-10: G12
WORLD HEALTH ORGANIZATION ICD-10: G12


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 distale autosomique récessive type 2

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




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amyotrophie spinale adulte

Date index:2021-02-18 -

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