Charcot–Marie–Tooth disease
Charcot–Marie–Tooth disease (CMT) is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle tissue and touch sensation across various parts of the body. This disease is the most commonly inherited neurological disorder affecting about one in 2,500 people. Currently, there are no curative treatments for this disorder, with care focused on maintaining function. CMT was previously classified as a subtype of muscular dystrophy.
known for
medical cause
AR-CMT2CMT2ACMT5CMT6CMTDCMTDICMTRICarcot marie toothCharcot-Marie-ToothCharcot-Marie-Tooth DiseaseCharcot-Marie-Tooth diseaseCharcot-Marie-Tooth disease, X-linked recessive, 4Charcot-Marie-Tooth disease, X-linked recessive type 5Charcot-Marie-Tooth disease, X-linked type 1Charcot-Marie-Tooth disease, X-linked type 2, recessiveCharcot-Marie-Tooth disease, X-linked type 2 recessiveCharcot-Marie-Tooth disease, X-linked type 3, recessiveCharcot-Marie-Tooth disease, X-linked type 3 recessiveCharcot-Marie-Tooth disease, neuronal, type ACharcot-Marie-Tooth disease, neuronal, type BCharcot-Marie-Tooth disease, neuronal, type DCharcot-Marie-Tooth disease, type 1Charcot-Marie-Tooth disease, type 2Charcot-Marie-Tooth disease, type 4Charcot-Marie-Tooth disease (neuronal form)Charcot-Marie-Tooth disease 2B1Charcot-Marie-Tooth disease and deafness deafness dominant typeCharcot-Marie-Tooth disease deafness dominant typeCharcot-Marie-Tooth disease deafness recessive typeCharcot-Marie-Tooth disease type 1Charcot-Marie-Tooth disease type 1ACharcot-Marie-Tooth disease type 1BCharcot-Marie-Tooth disease type 1CCharcot-Marie-Tooth disease type 1DCharcot-Marie-Tooth disease type 1ECharcot-Marie-Tooth disease type 1FCharcot-Marie-Tooth disease type 1 aplasia cutis congenitaCharcot-Marie-Tooth disease type 2Charcot-Marie-Tooth disease type 2ACharcot-Marie-Tooth disease type 2A1
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1884 in science1886 in science2019 in FranceA. Bartlett GiamattiAIFM1AR-CMT2Alan P. KozikowskiAlberto AbarzaAlcoholic polyneuropathyAlice LazzariniAlpha-tubulin N-acetyltransferaseAmyotrophic lateral sclerosisAndrew WyethAnkle jerk reflexAnne BertolottiAnterior grey columnArts syndromeAtrophyAuditory neuropathyBaclofenBen JessonCMTCMT2ACMT5CMT6CMTACMTDCMTDICMTRICOX10COX6A1CalnexinCarcot marie toothCarpal tunnel syndromeCauses of hearing lossCharcot-Marie-ToothCharcot-Marie-Tooth DiseaseCharcot-Marie-Tooth diseaseCharcot-Marie-Tooth disease, X-linked recessive, 4Charcot-Marie-Tooth disease, X-linked recessive type 5
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known for
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Charcot–Marie–Tooth disease
Charcot–Marie–Tooth disease (CMT) is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle tissue and touch sensation across various parts of the body. This disease is the most commonly inherited neurological disorder affecting about one in 2,500 people. Currently, there are no curative treatments for this disorder, with care focused on maintaining function. CMT was previously classified as a subtype of muscular dystrophy.
has abstract
A doença de Charcot-Marie-Toot ...... mação (ou descarte) da doença.
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Charcot-Marie-Tooths sjukdom ( ...... av genen PMP22 på kromosom 17.
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Charcot–Marie–Tooth disease (C ...... subtype of muscular dystrophy.
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Choroba Charcota-Mariego-Tooth ...... i Howarda Tootha (1856-1926).
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Der Morbus Charcot-Marie-Tooth ...... e dieser Erkrankung angesehen.
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Hereditaire motorische en sens ...... e neuropathieën zijn en (HNA).
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La enfermedad de Charcot-Marie ...... s tarde, hasta los 50-60 años.
@es
La malaltia de Charcot-Marie-T ...... iuen neuropaties perifèriques.
@ca
La malattia di Charcot-Marie-T ...... nte della distrofia muscolare.
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Les maladies de Charcot-Marie- ...... aussi progresser par poussées.
@fr
differential diagnosis
medical diagnosis
Wikipage page ID
page length (characters) of wiki page
Wikipage revision ID
1,019,025,887
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alt
Howard Henry Tooth
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Jean-Martin Charcot
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Pierre Marie
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caption
The foot of a person with Char ...... signs of this genetic disease.
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causes
Family history
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diagnosis
Genetic testing, nerve conduction study or electromyogram
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differential
duration
Lifelong
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frequency
image
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name
Charcot-Marie-Tooth disease
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onset
Childhood - early adulthood
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prognosis
progressive
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risks
Family history , high-arched feet, flat-arched feet
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symptoms
Foot drop, hammer toe, peripheral muscle wasting of lower legs
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synonyms
Charcot–Marie–Tooth neuropathy, peroneal muscular atrophy, Dejerine-Sottas Syndrome
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treatment
management to maintain function
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hypernym
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A doença de Charcot-Marie-Toot ...... mbém pode progredir em surtos.
@pt
Charcot-Marie-Tooths sjukdom ( ...... ning. Den vanligaste formen CM
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Charcot–Marie–Tooth disease (C ...... subtype of muscular dystrophy.
@en
Choroba Charcota-Mariego-Tooth ...... i Howarda Tootha (1856-1926).
@pl
Der Morbus Charcot-Marie-Tooth ...... e dieser Erkrankung angesehen.
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Hereditaire motorische en sens ...... aardoor een eigen naam, zoals
@nl
La enfermedad de Charcot-Marie ...... s tarde, hasta los 50-60 años.
@es
La malaltia de Charcot-Marie-T ...... iuen neuropaties perifèriques.
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La malattia di Charcot-Marie-T ...... tin Charcot, Pierre Marie, e .
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Les maladies de Charcot-Marie- ...... e qui est beaucoup plus grave.
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label
Charcot-Marie-Tooths sjukdom
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Charcot–Marie–Tooth disease
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Choroba Charcota-Mariego-Tootha
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Doença de Charcot-Marie-Tooth
@pt
Hereditaire motorische en sensorische neuropathieën
@nl
Maladie de Charcot-Marie-Tooth
@fr
Malaltia de Charcot-Marie-Tooth
@ca
Malattia di Charcot-Marie-Tooth
@it
Morbus Charcot-Marie-Tooth
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Síndrome de Charcot-Marie-Tooth
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sameAs
wasDerivedFrom
isPrimaryTopicOf
name
Charcot-Marie-Tooth disease
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