Charcot-Marie-Tooth Disease [Charcotova-Marieova-Toothova nemoc]

topical
159
Terms

Charcot-Marie-Toothova choroba
Charcotova-Marieova-Toothova nemoc, typ I
Charcotova-Marieova-Toothova nemoc, typ Ia
Charcotova-Marieova-Toothova nemoc, typ Ib
CMT
hereditární motorické a senzitivní neuropatie, typ 1A
hereditární motorické a senzitivní neuropatie, typ 1B
hereditární motorické a senzitivní neuropatie, typ I
hereditární motorické a senzitivní neuropatie, typ II
HMSN typ I
HMSN typ II
syndrom Roussy-Levyové

 

Atrophy, Muscular, Peroneal
Charcot-Marie Disease
Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A
Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B
Charcot-Marie-Tooth Disease, Demyelinating, Type 1A
Charcot-Marie-Tooth Disease, Demyelinating, Type 1B
Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy
Charcot-Marie-Tooth Disease, Type 1A
Charcot-Marie-Tooth Disease, Type 1B
Charcot-Marie-Tooth Disease, Type I
Charcot-Marie-Tooth Disease, Type IA
Charcot-Marie-Tooth Disease, Type IB
Charcot-Marie-Tooth Disease, Type II
Charcot-Marie-Tooth Hereditary Neuropathy
Charcot-Marie-Tooth Neuropathy, Type 1A
Charcot-Marie-Tooth Neuropathy, Type 1B
Charcot-Marie-Tooth Syndrome
Hereditary Areflexic Dystasia
Hereditary Motor and Sensory Neuropathy 1A
Hereditary Motor and Sensory Neuropathy 1B
Hereditary Motor and Sensory Neuropathy IA
Hereditary Motor And Sensory Neuropathy IB
Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor, and Sensory Neuropathy Type I
Hereditary Type I Motor and Sensory Neuropathy
HMN Distal Type I
HMSN 1A
HMSN 1B
HMSN I
HMSN IA
HMSN IB
HMSN II
HMSN Type I
HMSN Type II
HMSN1A
HMSN1B
Muscular Atrophy, Peroneal
Neuropathy, Type I Hereditary Motor and Sensory
Neuropathy, Type II Hereditary Motor and Sensory
Peroneal Muscular Atrophy
Roussy Levy Hereditary Areflexic Dystasia
Roussy-Levy Disease
Roussy-Levy Hereditary Areflexic Dystasia
Roussy-Levy Syndrome

Persistent link   https://www.medvik.cz/link/D002607
Definition

A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)

DUI
D002607 MeSH Browser
CUI
M0003994
History note
2000(1966)
Public note
2000; see CHARCOT-MARIE DISEASE 1991-1999, see MUSCULAR ATROPHY, SPINAL 1988-1990, see MUSCULAR ATROPHY 1966-1987; for CHARCOT-MARIE-TOOTH DISEASE see CHARCOT-MARIE DISEASE 1991-1999

Allowable subheadings

BL
blood 2
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 9
CO
complications 10
DI
diagnosis 63
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 2
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 2
EH
ethnology 4
ET
etiology 11
GE
genetics 85
HI
history
IM
immunology
ME
metabolism 5
MI
microbiology 1
MO
mortality 1
NU
nursing 1
PS
parasitology
PA
pathology 16
PP
physiopathology 15
PC
prevention & control 1
PX
psychology 3
RT
radiotherapy
RH
rehabilitation 9
SU
surgery 5
TH
therapy 29
UR
urine
VE
veterinary
VI
virology

C Diseases
C10 Nervous System Diseases 1 878
C10.500 Nervous System Malformations 80
C10.500.300 Hereditary Sensory and Motor Neuropathy 71
C10.500.300.099 Alstrom Syndrome 1
C10.500.300.200 Charcot-Marie-Tooth Disease 159
C10.500.300.490 Giant Axonal Neuropathy 1
C10.500.300.780 Refsum Disease 6
C10.500.300.820 Spastic Paraplegia, Hereditary 23
C10.574 Neurodegenerative Diseases 641
C10.574.500 Heredodegenerative Disorders, Nervous System 45
C10.574.500.495 Hereditary Sensory and Motor Neuropathy 71
C10.574.500.495.099 Alstrom Syndrome 1
C10.574.500.495.200 Charcot-Marie-Tooth Disease 159
C10.574.500.495.490 Giant Axonal Neuropathy 1
C10.574.500.495.780 Refsum Disease 6
C10.574.500.495.820 Spastic Paraplegia, Hereditary 23
C10.668 Neuromuscular Diseases 330
C10.668.829 Peripheral Nervous System Diseases 491
C10.668.829.800 Polyneuropathies 343
C10.668.829.800.300 Hereditary Sensory and Motor Neuropathy 71
C10.668.829.800.300.099 Alstrom Syndrome 1
C10.668.829.800.300.200 Charcot-Marie-Tooth Disease 159
C10.668.829.800.300.490 Giant Axonal Neuropathy 1
C10.668.829.800.300.780 Refsum Disease 6
C10.668.829.800.300.820 Spastic Paraplegia, Hereditary 23
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 741
C16.131.666 Nervous System Malformations 80
C16.131.666.300 Hereditary Sensory and Motor Neuropathy 71
C16.131.666.300.099 Alstrom Syndrome 1
C16.131.666.300.200 Charcot-Marie-Tooth Disease 159
C16.131.666.300.490 Giant Axonal Neuropathy 1
C16.131.666.300.780 Refsum Disease 6
C16.131.666.300.820 Spastic Paraplegia, Hereditary 23
C16.320 Genetic Diseases, Inborn 1 213
C16.320.400 Heredodegenerative Disorders, Nervous System 45
C16.320.400.375 Hereditary Sensory and Motor Neuropathy 71
C16.320.400.375.099 Alstrom Syndrome 1
C16.320.400.375.200 Charcot-Marie-Tooth Disease 159
C16.320.400.375.490 Giant Axonal Neuropathy 1
C16.320.400.375.780 Refsum Disease 6
C16.320.400.375.820 Spastic Paraplegia, Hereditary 23

Charcot Marie Tooth type 1 aplasia cutis congenita Disease MeSH Browser

Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k Disease MeSH Browser

Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Disease MeSH Browser

Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Disease MeSH Browser

Charcot-Marie-Tooth Disease, Axonal, Type 2n Disease MeSH Browser

Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Disease MeSH Browser

Charcot-Marie-Tooth Disease, Dominant Intermediate A Disease MeSH Browser

Charcot-Marie-Tooth Disease, Dominant Intermediate B Disease MeSH Browser

Charcot-Marie-Tooth Disease, Dominant Intermediate C Disease MeSH Browser

Charcot-Marie-Tooth Disease, Dominant Intermediate D Disease MeSH Browser

Charcot-Marie-Tooth Disease, Foot Deformity of Disease MeSH Browser

Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type Disease MeSH Browser

Charcot-Marie-Tooth Disease, Recessive Intermediate A Disease MeSH Browser

Charcot-Marie-Tooth Disease, Type 4H Disease MeSH Browser

Charcot-Marie-Tooth Disease, Type 4j Disease MeSH Browser

Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia Disease MeSH Browser

Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma Disease MeSH Browser

Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined Disease MeSH Browser

Charcot-Marie-Tooth disease and deafness Disease MeSH Browser

Charcot-Marie-Tooth disease with ptosis and parkinsonism Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 1C Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 1D Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 1E Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 1F Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2A Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2B Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2B1 Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2B2 Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2C Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2D Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2E Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2F Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2H Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2I Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2J Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 2K Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 4A Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 4A, axonal form Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 4B1 Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 4B2 Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 4C Disease MeSH Browser

Charcot-Marie-Tooth disease, Type 4E Disease MeSH Browser

Charcot-Marie-Tooth disease, X-linked recessive, 2 Disease MeSH Browser

Charcot-Marie-Tooth disease, X-linked recessive, 3 Disease MeSH Browser

Charcot-Marie-Tooth disease, X-linked, 1 Disease MeSH Browser

Charcot-Marie-Tooth disease, dominant intermediate 1 Disease MeSH Browser

Charcot-Marie-Tooth disease, dominant intermediate 2 Disease MeSH Browser

Charcot-Marie-Tooth disease, dominant intermediate 3 Disease MeSH Browser

Cowchock syndrome Disease MeSH Browser

Hereditary Motor And Sensory Neuropathy, Type IIC Disease MeSH Browser

Keratoderma palmoplantar spastic paralysis Disease MeSH Browser

Neuropathy, Distal Hereditary Motor, Type IIA Disease MeSH Browser

Neuropathy, hereditary motor and sensory, LOM type Disease MeSH Browser

Polyneuropathy, Mixed, of Early Onset Disease MeSH Browser

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