Hereditary Sensory and Motor Neuropathy [hereditární motorické a senzitivní neuropatie]

topical
71
Terms

Charcotova-Marieova-Toothova nemoc, typ 3
Charcotova-Marieova-Toothova nemoc, typ III
dědičné motorické a senzorické neuropatie
Déjerineova-Sottasova nemoc
hereditární motorické a senzitivní neuropatie, typ VII
hereditární motoricko-senzorické neuropatie
hereditární motoricko-senzorické neuropatie, typ III
HMN - proximální typ I
HMSN
HMSN typ III
HMSN typ VII
infantilní spinální svalová atrofie
morbus Werdnig-Hoffmann
nemoc Werdnigova-Hoffmannova
SMA typ 1
spinální svalová atrofie I. typu
Werdnigův-Hoffmannův typ SMA

 

Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
Charcot-Marie-Tooth Disease, Type 3
CMT4f
Dejerine-Sottas Disease
Dejerine-Sottas Neuropathy
Dejerine-Sottas Syndrome
Herditary Sensory and Motor Neuropathy
Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathy
Hereditary Motor and Sensory Neuropathy 3
Hereditary Motor and Sensory Neuropathy Type III
Hereditary, Type III, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy
HMN (Hereditary Motor Neuropathy) Proximal Type I
HMSN
HMSN Type III
HMSN Type VII
HMSN3
Hypertrophic Neuropathy of Dejerine-Sottas
Neuropathies, Hereditary Motor and Sensory
Proximal Hereditary Motor Neuropathy Type I

Persistent link   https://www.medvik.cz/link/D015417
Definition

A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)

Annotation
do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES
DUI
D015417 MeSH Browser
CUI
M0023767
Previous indexing
Charcot-Marie Disease (1975-1988); Muscular Atrophy (1972-1988); Neuromuscular Diseases (1979-1988)
History note
2000(1989); for HMN (HEREDITARY MOTOR NEUROPATHY) PROXIMAL TYPE I use SPINAL MUSCULAR ATROPHIES OF CHILDHOOD 1988-2025
Public note
2000; see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1988-1999, for HMN (HEREDITARY MOTOR NEUROPATHY) PROXIMAL TYPE I see SPINAL MUSCULAR ATROPHIES OF CHILDHOOD 1988-2025,

Allowable subheadings

BL
blood 1
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 10
CO
complications 4
DI
diagnosis 39
DG
diagnostic imaging 0
DH
diet therapy 0
DT
drug therapy 2
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 2
EH
ethnology 1
ET
etiology 6
GE
genetics 29
HI
history 0
IM
immunology 0
ME
metabolism 0
MI
microbiology 0
MO
mortality 1
NU
nursing 1
PS
parasitology 0
PA
pathology 5
PP
physiopathology 6
PC
prevention & control 0
PX
psychology 0
RT
radiotherapy 0
RH
rehabilitation 4
SU
surgery 2
TH
therapy 16
UR
urine 0
VE
veterinary 0
VI
virology 0

C Diseases
C10 Nervous System Diseases 1 877
C10.500 Nervous System Malformations 80
C10.500.034 Agenesis of Corpus Callosum 12
C10.500.142 Central Nervous System Cysts 27
C10.500.190 Central Nervous System Vascular Malformations 20
C10.500.198 Congenital Cranial Dysinnervation Disorders
C10.500.205 Dandy-Walker Syndrome 6
C10.500.250 Hereditary Sensory and Autonomic Neuropathies 26
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
C10.500.450 Hydranencephaly 3
C10.500.507 Malformations of Cortical Development 48
C10.500.680 Neural Tube Defects 77
C10.500.760 Optic Nerve Hypoplasia 1
C10.574 Neurodegenerative Diseases 641
C10.574.500 Heredodegenerative Disorders, Nervous System 45
C10.574.500.024 Alexander Disease 6
C10.574.500.050 Amyloid Neuropathies, Familial 20
C10.574.500.175 Bulbo-Spinal Atrophy, X-Linked 8
C10.574.500.300 Canavan Disease 9
C10.574.500.362 Cockayne Syndrome 4
C10.574.500.393 Dystonia Musculorum Deformans 3
C10.574.500.425 Gerstmann-Straussler-Scheinker Disease 22
C10.574.500.487 Hepatolenticular Degeneration 243
C10.574.500.490 Hereditary Central Nervous System Demyelinating Diseases 11
C10.574.500.493 Hereditary Sensory and Autonomic Neuropathies 26
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
C10.574.500.497 Huntington Disease 322
C10.574.500.529 Lafora Disease 1
C10.574.500.545 Myotonia Congenita 17
C10.574.500.547 Myotonic Dystrophy 94
C10.574.500.549 Neurofibromatoses 28
C10.574.500.550 Neuronal Ceroid-Lipofuscinoses 29
C10.574.500.662 Optic Atrophies, Hereditary 5
C10.574.500.700 Pantothenate Kinase-Associated Neurodegeneration 17
C10.574.500.812 Spinal Muscular Atrophies of Childhood 59
C10.574.500.825 Spinocerebellar Degenerations 30
C10.574.500.850 Tourette Syndrome 86
C10.574.500.865 Tuberous Sclerosis 141
C10.574.500.875 Unverricht-Lundborg Syndrome 1
C10.668 Neuromuscular Diseases 330
C10.668.829 Peripheral Nervous System Diseases 491
C10.668.829.800 Polyneuropathies 342
C10.668.829.800.050 Alcoholic Neuropathy 18
C10.668.829.800.175 Hereditary Sensory and Autonomic Neuropathies 26
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
C10.668.829.800.662 Paraneoplastic Polyneuropathy 14
C10.668.829.800.700 POEMS Syndrome 34
C10.668.829.800.750 Polyradiculoneuropathy 68
C10.668.829.800.875 Tangier Disease 3
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 740
C16.131.666 Nervous System Malformations 80
C16.131.666.034 Agenesis of Corpus Callosum 12
C16.131.666.142 Central Nervous System Cysts 27
C16.131.666.190 Central Nervous System Vascular Malformations 20
C16.131.666.198 Congenital Cranial Dysinnervation Disorders
C16.131.666.205 Dandy-Walker Syndrome 6
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
C16.131.666.310 Hereditary Sensory and Autonomic Neuropathies 26
C16.131.666.450 Hydranencephaly 3
C16.131.666.507 Malformations of Cortical Development 48
C16.131.666.680 Neural Tube Defects 77
C16.131.666.763 Optic Nerve Hypoplasia 1
C16.320 Genetic Diseases, Inborn 1 213
C16.320.400 Heredodegenerative Disorders, Nervous System 45
C16.320.400.024 Alexander Disease 6
C16.320.400.050 Amyloid Neuropathies, Familial 20
C16.320.400.100 Bulbo-Spinal Atrophy, X-Linked 8
C16.320.400.150 Canavan Disease 9
C16.320.400.200 Cockayne Syndrome 4
C16.320.400.330 Dystonia Musculorum Deformans 3
C16.320.400.350 Gerstmann-Straussler-Scheinker Disease 22
C16.320.400.361 Hepatolenticular Degeneration 243
C16.320.400.367 Hereditary Central Nervous System Demyelinating Diseases 11
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
C16.320.400.415 Hereditary Sensory and Autonomic Neuropathies 26
C16.320.400.430 Huntington Disease 322
C16.320.400.480 Lafora Disease 1
C16.320.400.525 X-Linked Intellectual Disability 17
C16.320.400.540 Myotonia Congenita 17
C16.320.400.542 Myotonic Dystrophy 94
C16.320.400.550 Neuroacanthocytosis 6
C16.320.400.560 Neurofibromatoses 28
C16.320.400.600 Neuronal Ceroid-Lipofuscinoses 29
C16.320.400.630 Optic Atrophies, Hereditary 5
C16.320.400.650 Pantothenate Kinase-Associated Neurodegeneration 17
C16.320.400.765 Spinal Muscular Atrophies of Childhood 59
C16.320.400.780 Spinocerebellar Degenerations 30
C16.320.400.820 Tourette Syndrome 86
C16.320.400.880 Tuberous Sclerosis 141
C16.320.400.940 Unverricht-Lundborg Syndrome 1

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