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Translation of "pyramid scheme " (English → French) :

Spinocerebellar ataxia type 31 (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense,
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ataxie spinocérébelleuse type 31
SNOMEDCT-BE (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense, / 715826005
SNOMEDCT-BE (disorder) / 715826005
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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
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syndrome neurodégénératif sévère avec lipodystrophie
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
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https://browser.ihtsdotools.or (...) [HTML]
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
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syndrome autosomique récessif de leucoencéphalopathie-infarctus cérébraux-rétinite pigmentaire
SNOMEDCT-BE (hypertelorism, a / 771476007
SNOMEDCT-BE (disorder) / 771476007
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https://browser.ihtsdotools.or (...) [HTML]
Main features described as cerebellar ataxia and cognitive dysfunction in almost three quarters of patients and pyramidal and sensory signs in approximately a third of patients. Other features include dysexecutive disorders and commonly psychiatric d
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ataxie spinocérébelleuse type 8
SNOMEDCT-BE (disorder) / 715753001
SNOMEDCT-BE (disorder) / 715753001
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https://browser.ihtsdotools.or (...) [HTML]
A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on br
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maladie de Huntington-like 3
SNOMEDCT-BE (on br / 770939009
SNOMEDCT-BE (disorder) / 770939009
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https://browser.ihtsdotools.or (...) [HTML]
Disease with characteristics of early-onset cerebellar signs, eye movement abnormalities and pyramidal signs. Fifty-one clinically affected members from four families (of British, Pakistani, German and French descent) have been reported to date. The
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ataxie spinocérébelleuse type 11
SNOMEDCT-BE (of British, Pakistani, German and French descent) have been reported to date. The / 719207000
SNOMEDCT-BE (disorder) / 719207000
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https://browser.ihtsdotools.or (...) [HTML]
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
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syndrome d'ataxie cérébelleuse autosomique récessive-signes pyramidaux-nystagmus-apraxie oculomotrice
SNOMEDCT-BE (disorder) / 763312008
SNOMEDCT-BE (disorder) / 763312008
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https://browser.ihtsdotools.or (...) [HTML]
Main features described as slowly progressive cerebellar syndrome and epilepsy, sometimes mild pyramidal signs, peripheral neuropathy and neuropsychological disturbances. Prevalence is unknown. Many kindreds have been found in Mexican and Brazilian p
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ataxie spinocérébelleuse type 10
SNOMEDCT-BE (disorder) / 715754007
SNOMEDCT-BE (disorder) / 715754007
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https://browser.ihtsdotools.or (...) [HTML]
A very rare progressive and untreatable disease with manifestations of ataxia with sensory neuropathy. Prevalence is unknown, typically starts in middle-aged adults and presents with cerebellar ataxia, pyramidal signs, and peripheral sensory loss. Th
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ataxie spinocérébelleuse type 4
SNOMEDCT-BE (disorder) / 715755008
SNOMEDCT-BE (disorder) / 715755008
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https://browser.ihtsdotools.or (...) [HTML]
A rare hereditary ataxia with characteristics of progressive cerebellar ataxia associated with disruption of visual fixation by saccadic intrusions. It presents with progressive gait, trunk and limb ataxia with pyramidal tract signs (increased tendon
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syndrome d'ataxie cérébelleuse autosomique récessive-saccade oculaire
SNOMEDCT-BE (increased tendon / 766814006
SNOMEDCT-BE (disorder) / 766814006
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https://browser.ihtsdotools.or (...) [HTML]


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Date index:2021-02-21 -

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