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Amyotrophie spinale
Distale
Fazio-Londe
Forme scapulo-péronière
Kugelberg-Welander
Myopathie distale précoce type Laing
Myopathie distale tardive type Markesbery-Griggs
Myopathie distale type Welander
Paralysie bulbaire progressive de l'enfant

Translation of "Myopathie distale type Welander " (French → English) :

myopathie distale type Welander

A distal myopathy with characteristics of weakness in the distal upper extremities usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremities primarily in toe and ankle extensors. This disease is mainly
SNOMEDCT-BE (disorder) / 726107008
SNOMEDCT-BE (disorder) / 726107008


myopathie distale précoce type Laing

Gowers disease
SNOMEDCT-BE (disorder) / 764859001
SNOMEDCT-BE (disorder) / 764859001


myopathie distale avec atteinte initiale des membres supérieurs type finlandais

Distal myopathy type 3
SNOMEDCT-BE (disorder) / 763718009
SNOMEDCT-BE (disorder) / 763718009


myopathie distale tardive type Markesbery-Griggs

ZASP related myofibrillar myopathy
SNOMEDCT-BE (disorder) / 770558006
SNOMEDCT-BE (disorder) / 770558006


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




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Myopathie distale type Welander

Date index:2023-04-07 -

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