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Hypokaliémique
Myotonique
Normokaliémique
Paralysie périodique
Paralysie périodique
Paralysie périodique familiale
Paralysie périodique hypokaliémique familiale
Paralysies périodiques
Primitive

Translation of "paralysie périodique familiale " (French → English) :

paralysie périodique familiale

Cavarre disease
SNOMEDCT-BE (disorder) / 267607008
SNOMEDCT-BE (disorder) / 267607008


Paralysie périodique (familiale):hyperkaliémique | hypokaliémique | myotonique | normokaliémique

Periodic paralysis (familial):hyperkalaemic | hypokalaemic | myotonic | normokalaemic
WORLD HEALTH ORGANIZATION ICD-10: G72.3
WORLD HEALTH ORGANIZATION ICD-10: G72.3


paralysie périodique hypokaliémique familiale

Periodic paralysis I
SNOMEDCT-BE (disorder) / 82732003
SNOMEDCT-BE (disorder) / 82732003


paralysie périodique avec neuropathie motrice distale tardive

A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy.
SNOMEDCT-BE (disorder) / 774154008
SNOMEDCT-BE (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy. / 774154008


paralysie périodique avec pseudo-syndrome des loges transitoire

A rare genetic neuromuscular disease characterised by normokalaemic episodes of painful muscle cramping followed by progressive permanent flaccid weakness. Triggered by stress, cold and exercise and associated with myopathic myopathy and painful acut
SNOMEDCT-BE (disorder) / 774153002
SNOMEDCT-BE (disorder) / 774153002


Paralysies périodiques

Periodic paralysis
WORLD HEALTH ORGANIZATION ICD-10: G72.3
WORLD HEALTH ORGANIZATION ICD-10: G72.3


paralysie périodique

Periodic paralysis
SNOMEDCT-BE (finding) / 198030008
SNOMEDCT-BE (finding) / 198030008


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

Familial motor neuron disease Lateral sclerosis:amyotrophic | primary | Progressive:bulbar palsy | spinal muscular atrophy
WORLD HEALTH ORGANIZATION ICD-10: G12.2
WORLD HEALTH ORGANIZATION ICD-10: G12.2




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paralysie périodique familiale

Date index:2023-02-24 -

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