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Translation of "Seizures " (English → Dutch) :
TERMINOLOGY
see also In-Context Translations below A rare neuroimmunological disorder characterized by the onset of cognitive decline, psychiatric disturbances and seizures (distinctively faciobrachial dystonic seizures) in association with detection of LGI1 antibodies in serum or cerebrospinal fluid
limbische encefalitis met LGI1-antilichamen
SNOMEDCT-NL (distinctively faciobrachial dystonic seizures) in association with detection of LGI1 antibodies in serum or cerebrospinal fluid / 763794005
SNOMEDCT-NL (aandoening) / 763794005
A rare genetic neurologic disease with characteristics of congenital microcephaly, severe early-onset epileptic encephalopathy (manifesting as intractable, myoclonic and/or tonic-clonic seizures), permanent neonatal, insulin-dependent diabetes mellit
syndroom van primaire microcefalie, epilepsie en permanente neonatale diabetes
SNOMEDCT-NL (manifesting as intractable, myoclonic and/or tonic-clonic seizures), permanent neonatal, insulin-dependent diabetes mellit / 782825008
SNOMEDCT-NL (aandoening) / 782825008
Syndrome with characteristics of infancy onset hypotonia, feeding difficulties, breathing problems, dysphagia, severely delayed development of speech and motor skills, distinctive facial features, recurrent seizures and seizure-like episodes (muscle
5q31.3-microdeletiesyndroom
SNOMEDCT-NL (muscle / 768555009
SNOMEDCT-NL (aandoening) / 768555009
A rare genetic neurometabolic disease with characteristics of encephalomyopathy (including developmental delay, nystagmus, progressive ataxia, dystonia, amyotrophy, visual loss, sensorineural deafness, seizures) and bilateral symmetrical lesions in t
Leigh-syndroom met nefrotisch syndroom
SNOMEDCT-NL (including developmental delay, nystagmus, progressive ataxia, dystonia, amyotrophy, visual loss, sensorineural deafness, seizures) and bilateral symmetrical lesions in t / 783157004
SNOMEDCT-NL (aandoening) / 783157004
A rare epilepsy syndrome characterised by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behaviour problems are frequentl
cryptogene epileptische spasmen met late aanvang
SNOMEDCT-BE (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently / 778063003
SNOMEDCT-BE (disorder) / 778063003
A form of familial primary hypomagnesemia characterized by low serum magnesium values but inappropriate normal urinary magnesium values (i.e. renal hypomagnesemia). The typical symptoms are weakness of the limbs, vertigo, headaches, seizures, brisk t
familiale primaire hypomagnesiëmie met normocalciurie en normocalcïemie
SNOMEDCT-BE (i.e. renal hypomagnesemia). The typical symptoms are weakness of the limbs, vertigo, headaches, seizures, brisk t / 725031005
SNOMEDCT-BE (disorder) / 725031005
Jeavons syndrome is an idiopathic generalised form of reflex epilepsy characterised by childhood onset, unique seizure manifestations, striking light sensitivity, and possible occurrence of generalised tonic-clonic seizures. Onset occurs in childhood
Jeavons-syndroom
SNOMEDCT-BE (disorder) / 716278005
SNOMEDCT-BE (disorder) / 716278005
A rare epilepsy syndrome characterized by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently
infantiele spasmen met late aanvang
SNOMEDCT-BE (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently / 778063003
SNOMEDCT-BE (disorder) / 778063003
Progressive cavitating leukoencephalopathy has characteristics of acute episodes of neurological deficit (ataxia, dysarthria, seizures) with irritability and opisthotonus followed by either steady deterioration or alternating periods of rapid progres
progressieve caviterende leuko-encefalopathie
SNOMEDCT-BE (ataxia, dysarthria, seizures) with irritability and opisthotonus followed by either steady deterioration or alternating periods of rapid progres / 719267003
SNOMEDCT-BE (disorder) / 719267003
Disease with characteristics of recurrent seizures and profound disruption of brain development. Onset is within the first few weeks after birth. The seizures tend to be refractory to treatment. Most affected children have severe intellectual disabil
GM3-synthasedeficiëntie
SNOMEDCT-NL (aandoening) / 722762005
SNOMEDCT-NL (aandoening) / 722762005
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'Seizures'
Date index:2022-06-07 -
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