Hereditary motor and sensory neuropathy
Hereditary motor and sensory neuropathies (HMSN) is a name sometimes given to a group of different neuropathies which are all characterized by their impact upon both afferent and efferent neural communication. HMSN are characterised by atypical neural development and degradation of neural tissue. The two common forms of HMSN are either hypertrophic demyelinated nerves or complete atrophy of neural tissue. Hypertrophic condition causes neural stiffness and a demyelination of nerves in the peripheral nervous system, and atrophy causes the breakdown of axons and neural cell bodies. In these disorders, a patient experiences progressive muscle atrophy and sensory neuropathy of the extremities.
HMSNHereditary Motor Sensory NeuropathyHereditary Motor and Sensory NeuropathyHereditary Sensory & Motor NeuropathyHereditary Sensory Motor NeuropathyHereditary Sensory and Motor NeuropathyHereditary motor and sensory neuropathiesHereditary motor sensory neuropathyHereditary sensorimotor neuropathyHereditary sensory and motor neuropathyHereditary sensory motor neuropathy
Wikipage redirect
Charcot–Marie–Tooth diseaseCharcot–Marie–Tooth disease classificationsDistal hereditary motor neuronopathiesEoghan CliffordHMSNHereditary Motor Sensory NeuropathyHereditary Motor and Sensory NeuropathyHereditary Sensory & Motor NeuropathyHereditary Sensory Motor NeuropathyHereditary Sensory and Motor NeuropathyHereditary motor and sensory neuropathiesHereditary motor and sensory neuropathy with proximal dominanceHereditary motor sensory neuropathyHereditary neuropathy with liability to pressure palsyHereditary sensorimotor neuropathyHereditary sensory and autonomic neuropathy type IHereditary sensory and motor neuropathyHereditary sensory motor neuropathyList of MeSH codes (C10)List of MeSH codes (C16)Motor neuron diseasePierre MarieSLC25A46Spinal muscular atrophies
Link from a Wikipage to another Wikipage
primaryTopic
Hereditary motor and sensory neuropathy
Hereditary motor and sensory neuropathies (HMSN) is a name sometimes given to a group of different neuropathies which are all characterized by their impact upon both afferent and efferent neural communication. HMSN are characterised by atypical neural development and degradation of neural tissue. The two common forms of HMSN are either hypertrophic demyelinated nerves or complete atrophy of neural tissue. Hypertrophic condition causes neural stiffness and a demyelination of nerves in the peripheral nervous system, and atrophy causes the breakdown of axons and neural cell bodies. In these disorders, a patient experiences progressive muscle atrophy and sensory neuropathy of the extremities.
has abstract
Hereditary motor and sensory n ...... N is now used less frequently.
@en
eMedicine subject
neuro
@en
eMedicine topic
468
@en
MeSH ID
Wikipage page ID
17,595,947
Link from a Wikipage to a Wikipage in a different language about the same or a related subject.
page length (characters) of wiki page
Wikipage revision ID
976,191,449
Link from a Wikipage to another Wikipage
caption
Onion bulb formations in a nerve biopsy in a case of HMSN type I
@en
eMedicineSubj
neuro
@en
eMedicineTopic
MeshID
D015417
@en
name
Hereditary motor and sensory neuropathy
@en
wikiPageUsesTemplate
wordnet_type
hypernym
comment
Hereditary motor and sensory n ...... neuropathy of the extremities.
@en
label
Hereditary motor and sensory neuropathy
@en
sameAs
isPrimaryTopicOf
name
Hereditary motor and sensory neuropathy
@en