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Translation of "brain disease " (English → French) :
TERMINOLOGY
see also In-Context Translations below encephalopathy | brain disease
encéphalopathie | affection du cerveau
UGENT - Medical terms -
UGENT - Medical terms -
A mitochondrial disease due to a defect in mitochondrial protein synthesis resulting in deficiency of respiratory chain complexes I, III and IV in the cardiac and skeletal muscle and brain. The disease has characteristics of severe hypertrophic cardi
déficit combiné de la phosphorylation oxydative type 8
SNOMEDCT-BE (disorder) / 733600007
SNOMEDCT-BE (disorder) / 733600007
A disorder of the white matter of the brain causing neurological problems, which can occur, anytime from childhood to adulthood. Characteristics of the disease include learning disabilities, retinopathy, atrophy of the optic nerves, spasticity, infer
leucoencéphalopathie avec ataxie cérébelleuse modérée et oedème de la substance blanche
SNOMEDCT-BE (disorder) / 768663003
SNOMEDCT-BE (disorder) / 768663003
A polymorphic disorder with characteristics of ataxia, sensorineural deafness and narcolepsy with cataplexy and dementia. Disease onset occurs in adulthood from the ages of 30-40. Mild brain atrophy with cerebellum involvement is visible with magneti
syndrome d'ataxie cérébelleuse autosomique dominante-surdité-narcolepsie
SNOMEDCT-BE (disorder) / 722293005
SNOMEDCT-BE (disorder) / 722293005
A rare neurologic disease characterized by global developmental delay, intellectual disability, multiple ischemic lesions on brain MRI, behavioral abnormalities, dystonia, choreic movements and pyramidal syndrome, facial dysmorphism (hypertelorism, a
syndrome autosomique récessif de leucoencéphalopathie-infarctus cérébraux-rétinite pigmentaire
SNOMEDCT-BE (hypertelorism, a / 771476007
SNOMEDCT-BE (disorder) / 771476007
A chromosomal anomaly with characteristics of severe developmental delay and/or intellectual disability, typical facial dysmorphic features, brain anomalies, seizures, cleft palate, clubfeet, nail hypoplasia and congenital heart disease.
syndrome de microdélétion 1q41q42
SNOMEDCT-BE (disorder) / 716515000
SNOMEDCT-BE (disorder) / 716515000
A rare mitochondrial disorder due to a defect in mitochondrial protein synthesis characterised by severe intrauterine growth retardation, neonatal limb oedema and redundant skin on the neck (hydrops), developmental brain defects (corpus callosum agen
déficit combiné de la phosphorylation oxydative type 2
SNOMEDCT-BE (hydrops), developmental brain defects (corpus callosum agen / 764943000
SNOMEDCT-BE (disorder) / 764943000
A rare genetic leukodystrophy disorder with characteristics of diffuse hypomyelination in the supratentorial brain white matter, brain stem and spinal cord. Patients usually present nystagmus, lower limb spasticity, hypotonia and motor developmental
hypomyélinisation avec atteinte du tronc cérébral et de la moelle épinière et spasticité des jambes
SNOMEDCT-BE (disorder) / 777999008
SNOMEDCT-BE (disorder) / 777999008
A central nervous system malformation with characteristics of severe intellectual deficit, early hypotonia with progression to spasticity and contractures, choreoathetosis, seizures, dysmorphic face (long face with prominent forehead) and brain imagi
syndrome de déficience intellectuelle liée à l'X-malformation de Dandy-Walker-anomalies des noyaux gris centraux-convulsions
SNOMEDCT-BE (long face with prominent forehead) and brain imagi / 719139003
SNOMEDCT-BE (disorder) / 719139003
cerebellar | brain-related
cérébelleux | qui se rapporte au cervelet
UGENT - Medical terms -
UGENT - Medical terms -
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'brain disease'
Date index:2023-06-25 -
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