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

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

periodieke verlamming met voorbijgaand compartimentachtig syndroom

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

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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progressieve polyneuropathie met bilaterale striatale necrose

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

Flaccid tetraplegia

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

hypotone tetraplegie

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

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

Flaccid paraplegia

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

hypotone paraplegie

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

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

Anderen hebben gezocht naar : flaccid hemiplegia flaccid paraplegia flaccid tetraplegia alternate hemiplegia alternating hemiplegia crossed hemiplegia flaccid infantile spastic hemiplegia spastic hemiplegia

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'flaccid hemiplegia' ->

Date index: 2021-12-31