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Hemiplegia
Paralysis of one side
Spastic hemiplegia

Translation of "Spastic hemiplegia " (English → Dutch) :

Spastic hemiplegia
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spastische hemiplegie
SNOMEDCT-BE (disorder) / 79633009
SNOMEDCT-BE (disorder) / 79633009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Spastic hemiplegia
https://icd.who.int/browse10/2 (...) (...) [HTML]
hypertone hemiplegie
WORLD HEALTH ORGANIZATION ICD-10: G81.1
WORLD HEALTH ORGANIZATION ICD-10: G81.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://terminologie.nictiz.nl (...) [HTML]
hemiplegia | paralysis of one side
http://users.ugent.be/~rvdstic (...) (...) [HTML]
hemiplegie | halfzijdige verlamming
UGENT - Medical terms -
UGENT - Medical terms -
http://users.ugent.be/~rvdstic (...) (...) [HTML]
http://users.ugent.be/~rvdstic (...) [HTML]
AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
https://browser.ihtsdotools.or (...) (...) [HTML]
spastisch ataxie, myoclonische epilepsie, neuropathiesyndroom met vroege aanvang
SNOMEDCT-BE (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome / 771469002
SNOMEDCT-BE (disorder) / 771469002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Syndrome with characteristics of precocious puberty (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa
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spastische paraplegie, vroegtijdige puberteit
SNOMEDCT-BE (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa / 732958004
SNOMEDCT-BE (disorder) / 732958004
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A form of hereditary spastic paraplegia with onset usually in adulthood of progressive bilateral lower limb weakness and spasticity, sphincter dysfunction, decreased vibratory sense at the ankles and with additional manifestations including optical n
https://browser.ihtsdotools.or (...) (...) [HTML]
autosomaal recessieve spastische paraplegie type 7
SNOMEDCT-BE (disorder) / 715776003
SNOMEDCT-BE (disorder) / 715776003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Rare syndrome with the association of the features of Waardenburg Shah and neurological features namely neonatal hypotonia, intellectual deficit (of variable severity), nystagmus, progressive spasticity, ataxia and epilepsy. Autonomic dysfunction (re
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syndroom van perifere demyeliniserende neuropathie, centrale dysmyeliniserende leukodystrofie, syndroom van Waardenburg en ziekte van Hirschsprung
SNOMEDCT-NL (of variable severity), nystagmus, progressive spasticity, ataxia and epilepsy. Autonomic dysfunction (re / 765325002
SNOMEDCT-NL (aandoening) / 765325002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A progressive chronic inflammatory disease of the central nervous system with the aetiologic agent Human T cell lymphotropic virus type I (HTLV-I), the disease is characterised by unremitting myelopathic symptoms such as spastic paraparesis, bowel an
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myelopathie door infectie door humaan T-cel-lymfotroop virus type 1
SNOMEDCT-NL (HTLV-I), the disease is characterised by unremitting myelopathic symptoms such as spastic paraparesis, bowel an / 714279000
SNOMEDCT-NL (aandoening) / 714279000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A rare mitochondrial substrate carrier disorder with characteristics of severe muscular hypotonia, seizures beginning in the first year of life and arrested psychomotor development (affecting mainly motor skills). Severe spasticity with hyperreflexia
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epileptische encefalopathie met globale cerebrale demyelinisatie
SNOMEDCT-BE (affecting mainly motor skills). Severe spasticity with hyperreflexia / 726702005
SNOMEDCT-BE (disorder) / 726702005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A rare genetic neurodegenerative disorder characterized by progressive psychomotor and cognitive regression (manifesting with gait ataxia, spasticity, loss of language, mild to severe intellectual disability, pyramidal and extrapyramidal signs and, f
https://browser.ihtsdotools.or (...) (...) [HTML]
ernstig neurodegeneratief syndroom met lipodystrofie
SNOMEDCT-BE (manifesting with gait ataxia, spasticity, loss of language, mild to severe intellectual disability, pyramidal and extrapyramidal signs and, f / 773555005
SNOMEDCT-BE (disorder) / 773555005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : spastic hemiplegia    hemiplegia    paralysis of one side    Spastic hemiplegia    


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'Spastic hemiplegia'

Date index:2022-02-23 -

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