dystrophie musculaire de Duchenne | myopathie de Duchenne | myopathie primitive progressive pseudo-hypertrophique type Duchenne-Griesinger | myopathie pseudo-hypertrophique de Duchenne | DMD [Abbr.]

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IATE - Health

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dystrophie musculaire [ myopathie primitive | myopathie primitive progressive ]

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muscular dystrophy

Muscles et tendons

Muscles and Tendons

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atrophie de Duchenne-Friedreich | myopathie primitive progressive type pseudo-hypertrophique de Duchenne

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Duchenne-Friedreich atrophy

IATE - Health

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Amyotrophie spinale progressive Dégénérescence familiale du neurone moteur Paralysie bulbaire progressive Sclérose latérale:amyotrophique | primitive

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Familial motor neuron disease Lateral sclerosis:amyotrophic | primary | Progressive:bulbar palsy | spinal muscular atrophy

WORLD HEALTH ORGANIZATION ICD-10: G12.2

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Définition: La maladie d'Alzheimer est une maladie cérébrale dégénérative primitive d'étiologie inconnue dont la neuropathologie et la neurochimie sont caractéristiques. Elle débute habituellement de façon insidieuse et progresse lentement mais régulièrement en quelques années.

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Definition: Alzheimer's disease is a primary degenerative cerebral disease of unknown etiology with characteristic neuropathological and neurochemical features. The disorder is usually insidious in onset and develops slowly but steadily over a period of several years.

WORLD HEALTH ORGANIZATION ICD-10: F00*

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ophtalmoplégie externe progressive chronique de l'adulte avec myopathie mitochondriale

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A rare mitochondrial disease with characteristics of adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuro

SNOMEDCT-BE (disorder) / 725464001

SNOMEDCT-BE (e.g. impaired gait, dysarthria) and mild motor peripheral neuro / 725464001

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syndrome d'ophtalmoplégie externe progressive-myopathie-émaciation

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A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

SNOMEDCT-BE (disorder) / 764733009

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Others have searched : amyotrophie primitive progressive amyotrophie progressive atrophie de duchenne-friedreich atrophie musculaire progressive dystrophie musculaire dystrophie musculaire de duchenne dystrophie musculaire progressive myopathie atrophique progressive myopathie de duchenne myopathie primitive myopathie primitive progressive primitive

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myopathie primitive progressive

Date index:2021-02-13 -

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Translation of "myopathie primitive progressive " (French → English) :

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