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Déjerine-Sottas
Hypertrophique de l'enfant
Maladie de Charcot-Marie-Tooth liée à l'X type 4
Maladie de Charcot-Marie-Tooth type 4
Maladie de Charcot-Marie-Tooth type 4J
Syndrome de Roussy-Lévy

Translation of "maladie de charcot-marie-tooth type 4j " (French → English) :

TERMINOLOGY
see also In-Context Translations below
maladie de Charcot-Marie-Tooth type 4J
https://browser.ihtsdotools.or (...) (...) [HTML]
Charcot-Marie-Tooth disease type 4J
SNOMEDCT-BE (disorder) / 720638000
SNOMEDCT-BE (disorder) / 720638000
https://browser.ihtsdotools.or (...) (...) [HTML]
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]
maladie de Charcot-Marie-Tooth autosomique dominante type 2K
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2K
SNOMEDCT-BE (disorder) / 719512003
SNOMEDCT-BE (disorder) / 719512003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth type 4
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal recessive demyelinating Charcot-Marie-Tooth
SNOMEDCT-BE (disorder) / 715795005
SNOMEDCT-BE (disorder) / 715795005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth liée à l'X type 4
https://browser.ihtsdotools.or (...) (...) [HTML]
A rare genetic axonal peripheral sensorimotor neuropathy with an X-linked recessive inheritance pattern and the neonatal to early childhood-onset of severe, slowly progressive, distal muscle weakness and atrophy (in particular of the peroneal group)
SNOMEDCT-BE (disorder) / 763400005
SNOMEDCT-BE (in particular of the peroneal group) / 763400005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2N
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2N
SNOMEDCT-BE (disorder) / 719515001
SNOMEDCT-BE (disorder) / 719515001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2B
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2B
SNOMEDCT-BE (disorder) / 717008005
SNOMEDCT-BE (disorder) / 717008005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2D
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2D
SNOMEDCT-BE (disorder) / 717011006
SNOMEDCT-BE (disorder) / 717011006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2C
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2C
SNOMEDCT-BE (disorder) / 717010007
SNOMEDCT-BE (disorder) / 717010007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2L
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2L
SNOMEDCT-BE (disorder) / 719513008
SNOMEDCT-BE (disorder) / 719513008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS
Toutefois, plus de 50 % des maladies rares ne surviennent qu'à l'âge adulte, comme la maladie de Huntington, la maladie de Crohn, la maladie de Charcot-Marie-Tooth, la sclérose latérale amyotrophique, la maladie de Kapos ou le cancer de la thyroïde.
http://www.cihr-irsc.gc.ca/f/4 (...) (...) [HTML]
However, more than 50% of rare diseases only appear during adulthood, such as Huntington disease, Crohn's disease, Charcot-Marie-Tooth disease, amyotrophic lateral sclerosis, Kaposi's sarcoma, or thyroid cancer.
http://www.cihr-irsc.gc.ca/f/4 (...) (...) [HTML]
http://www.cihr-irsc.gc.ca/e/4 (...) [HTML]
Un gène défectueux en cause dans la SP Allison Kraus, étudiante au doctorat qui travaille au laboratoire du Dr Marek Michalak, découvre qu'un gène dysfonctionnel appelé calnexine semble contribuer à l'apparition de la sclérose en plaques et à un trouble connexe appelé maladie de Charcot-Marie-Tooth.
http://www.cihr-irsc.gc.ca/f/3 (...) (...) [HTML]
Linking faulty gene to MS Allison Kraus, a PhD student working with Dr. Marek Michalak, discovers that a misfiring gene called calnexin appears to contribute to multiple sclerosis and a related disorder called Charcot-Marie-Tooth disease.
http://www.cihr-irsc.gc.ca/f/3 (...) (...) [HTML]
http://www.cihr-irsc.gc.ca/e/3 (...) [HTML]


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maladie de charcot-marie-tooth type 4j

Date index:2023-09-22 -

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