Hereditary Sensory and Motor Neuropathy [hereditární motorické a senzitivní neuropatie]
- Terms
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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
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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
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
- CI
- chemically induced
- CL
- classification 10
- CO
- complications 4
- DI
- diagnosis 39
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 2
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 2
- EH
- ethnology 1
- ET
- etiology 6
- GE
- genetics 29
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality 1
- NU
- nursing 1
- PS
- parasitology
- PA
- pathology 5
- PP
- physiopathology 6
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation 4
- SU
- surgery 2
- TH
- therapy 16
- UR
- urine
- VE
- veterinary
- VI
- virology
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Hagemoser Weinstein Bresnick syndrome Disease MeSH Browser
Hereditary Motor And Sensory Neuropathy VI Disease MeSH Browser
Hypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy Disease MeSH Browser
Neuropathy, Distal Hereditary Motor, Type VIIA Disease MeSH Browser
Neuropathy, Hereditary Motor and Sensory, with Excessive Myelin Folding Complex, Autosomal Recessive Disease MeSH Browser
Neuropathy, Hereditary Sensorimotor, with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance Disease MeSH Browser
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Disease MeSH Browser
Neuropathy, Hereditary Thermosensitive Disease MeSH Browser
Neuropathy, hereditary motor and sensory, Okinawa type Disease MeSH Browser
Neuropathy, hereditary motor and sensory, Russe type Disease MeSH Browser
Polyneuropathy, Lethal Neonatal, Axonal Sensorimotor, Autosomal Recessive Disease MeSH Browser
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Disease MeSH Browser
Slowed Nerve Conduction Velocity, Autosomal Dominant Disease MeSH Browser
Spastic Paraplegia, Optic Atrophy, and Neuropathy Disease MeSH Browser
Tamari Goodman syndrome Disease MeSH Browser
Tomaculous neuropathy Disease MeSH Browser
Tremor hereditary essential, 2 Disease MeSH Browser