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

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paralysie périodique avec pseudo-syndrome des loges transitoire

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A rare genetic disorder of thiamine metabolism and transport with characteristics of the childhood-onset of recurrent episodes of flaccid paralysis and encephalopathy, associated with bilateral striatal necrosis and chronic progressive axonal polyneu

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polyneuropathie progressive avec nécrose striatale bilatérale

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Flaccid tetraplegia

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

Tétraplégie flasque

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

Flaccid paraplegia

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

Paraplégie flasque

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

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

D'autres ont cherché : flaccid hemiplegia flaccid paraplegia flaccid tetraplegia acute flaccid paralysis alternate hemiplegia alternating hemiplegia crossed hemiplegia flaccid palsy flaccid paralysis Flaccid hemiplegia

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'Flaccid hemiplegia' ->

Date index: 2020-12-14