Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie héréditaire sensitive et autonomique
Déjerine-Sottas
Récessive
Neuropathie motrice distale héréditaire type Jerash
Neuropathie sensitivomotrice héréditaire type 4
Neuropathie motrice distale héréditaire type 7
Neuropathie sensitivomotrice héréditaire de type I
Neuropathie sensitivo-motrice héréditaire type 5
Neuropathie motrice distale héréditaire type 1
Neuropathie sensitivo-motrice héréditaire type Okinawa

"neuropathie héréditaire sensitive et autonomique type 1 "

(French → English)
TERMINOLOGY
see also In-Context Translations below
neuropathie héréditaire sensitive et autonomique type 1 | neuropathie héréditaire sensitive et autonomique | Déjerine-Sottas | hypertrophique de l'enfant | Syndrome de Roussy-Lévy | récessive | Syndrome de Nélaton | neuropathie motrice distale héréditaire type Jerash | neuropathie sensitivomotrice héréditaire type 4 | neuropathie motrice distale héréditaire type 7 | neuropathie sensitivomotrice héréditaire de type I | neuropathie sensitivo-motrice héréditaire type 5 | neuropathie motrice distale héréditaire type 1 | neuropathie sensitivo-motrice héréditaire type Okinawa -*- Hereditary sensory and autonomic neuropathy type I | Hereditary sensory and autonomic neuropathy type 1B | Hereditary sensory and autonomic neuropathy | Disease:Charcot-Marie-Tooth | Déjerine-Sottas | recessively inherited | Refsum's disease | Distal hereditary motor neuropathy type 7

neuropathie héréditaire sensitive et autonomique type 1

Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008


neuropathie héréditaire sensitive et autonomique type 1B

Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008


neuropathie héréditaire sensitive et autonomique avec surdité et retard de développement

This syndrome has characteristics of sensory and autonomic axonal neuropathy, sensorineural hearing loss and persistent global developmental delay. It has been described in four individuals from a consanguineous Lebanese family. Onset occurred in inf
SNOMEDCT-BE (disorder) / 717826009


neuropathie héréditaire sensitive et autonomique

Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005


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

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


Maladie de Morvan Neuropathie sensitive héréditaire à transmission:dominante | récessive | Syndrome de Nélaton

Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited
WORLD HEALTH ORGANIZATION ICD-10: G60.8


neuropathie motrice distale héréditaire type Jerash

Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003


neuropathie sensitivomotrice héréditaire type 4

Refsum's disease
SNOMEDCT-BE (disorder) / 25362006


neuropathie motrice distale héréditaire type 7

Distal hereditary motor neuropathy type 7
SNOMEDCT-BE (disorder) / 771081007


neuropathie sensitivomotrice héréditaire de type I

HSMN, type I
SNOMEDCT-BE (disorder) / 398040009


neuropathie sensitivo-motrice héréditaire type 5

Charcot-Marie-Tooth disease, pyramidal features syndrome
SNOMEDCT-BE (disorder) / 771143004


neuropathie motrice distale héréditaire type 1

Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005


neuropathie sensitivo-motrice héréditaire type Okinawa

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
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 .

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.




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neuropathie héréditaire sensitive et autonomique type 1

Date index:2021-03-29
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