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Déjerine-Sottas
Hypertrophique de l'enfant
Neuropathie héréditaire motrice et sensorielle
Neuropathie motrice distale héréditaire type 1
Neuropathie motrice distale héréditaire type 7
Neuropathie motrice distale héréditaire type Jerash
Neuropathie sensitivo-motrice héréditaire type 5
Neuropathie sensitivo-motrice héréditaire type Okinawa
Syndrome de Roussy-Lévy

Translation of "neuropathie sensitivo-motrice héréditaire type 5 " (French → English) :

TERMINOLOGY
see also In-Context Translations below
neuropathie sensitivo-motrice héréditaire type 5
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Charcot-Marie-Tooth disease, pyramidal features syndrome
SNOMEDCT-BE (disorder) / 771143004
SNOMEDCT-BE (disorder) / 771143004
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https://browser.ihtsdotools.or (...) [HTML]
neuropathie sensitivo-motrice héréditaire type Okinawa
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An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high
SNOMEDCT-BE (disorder) / 715665006
SNOMEDCT-BE (disorder) / 715665006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie sensitivo-motrice axonale héréditaire avec acrodystrophie
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A rare axonal hereditary motor and sensory neuropathy with characteristics of progressive axonal neuropathy with limb weakness and severe distal sensory loss in all limbs and acrodystrophic changes leading to painless non-healing ulcers, osteomyeliti
SNOMEDCT-BE (disorder) / 771144005
SNOMEDCT-BE (disorder) / 771144005
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https://browser.ihtsdotools.or (...) [HTML]
syndrome de microcephalie-neuropathie sensitivo-motrice axonale complexe
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An extremely rare subtype of hereditary motor and sensory neuropathy with characteristics of severe, rapidly progressing, distal, symmetric polyneuropathy and microcephaly (which can be evident in utero) with intact cognition. Clinically it presents
SNOMEDCT-BE (disorder) / 763798008
SNOMEDCT-BE (which can be evident in utero) with intact cognition. Clinically it presents / 763798008
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https://browser.ihtsdotools.or (...) [HTML]
Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy
https://icd.who.int/browse10/2 (...) (...) [HTML]
Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
neuropathie motrice distale héréditaire type Jerash
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Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003
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https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire type 1
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Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire type 7
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Distal hereditary motor neuropathy type 7
SNOMEDCT-BE (disorder) / 771081007
SNOMEDCT-BE (disorder) / 771081007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Neuropathie héréditaire motrice et sensorielle
https://icd.who.int/browse10/2 (...) (...) [HTML]
Hereditary motor and sensory neuropathy
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
neuropathie motrice distale héréditaire de l'adulte jeune
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Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS
Ces nouvelles connaissances sont issues d'une étude subventionnée par les IRSC et intitulée « Le transporteur axonal des vésicules synaptiques K1F1A mute en neuropathie sensitive et autonomique héréditaire de type 2 », publiée dans la revue American Journal of Human Genetics .
http://www.cihr-irsc.gc.ca/f/4 (...) (...) [HTML]
The findings were reported in a study entitled " The axonal transporter of synaptic vesicles KIF1A is mutated in hereditary sensory and autonomic neuropathy type 2" . The study was published in the American Journal of Human Genetics and was supported by a grant from CIHR.
http://www.cihr-irsc.gc.ca/f/4 (...) (...) [HTML]
http://www.cihr-irsc.gc.ca/e/4 (...) [HTML]


Others have searched : déjerine-sottas    neuropathie héréditaire motrice et sensorielle    syndrome de roussy-lévy    hypertrophique de l'enfant    neuropathie sensitivo-motrice héréditaire type    neuropathie sensitivo-motrice héréditaire type okinawa    neuropathie sensitivo-motrice héréditaire type 5    


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neuropathie sensitivo-motrice héréditaire type 5

Date index:2022-11-21 -

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