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Mononeuritis multiplex

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Mononeuritis multiplex
ICD-10 G587
ICD-9 354.5
OMIM [1]
DiseasesDB 8346
MedlinePlus 000782
eMedicine pmr/80
MeSH {{{MeshNumber}}}


Mononeuritis multiplex is the clinical picture that arises from problems with multiple individual nerves serially or almost simultaneously.

Synonyms[]

Mononeuropathy multiplex

Clinical findings[]

Mononeuritis multiplex typically presents with the acute or subacute evolution of loss of sensory and motor function of individual peripheral nerves. The pattern of involvement is asymmetric.

Diagnosis[]

Electrodiagnostic studies will show multifocal sensory motor axonal neuropathy.

Causes and associations[]

See also[]


v·d·e
Nervous system pathology, primarily PNS (G50-G99, 350-359)
Nerve, nerve root
and plexus disorders

cranial nerve: V (Trigeminal neuralgia) - VII (Facial nerve paralysis, Bell's palsy, Melkersson-Rosenthal syndrome, Central seven) - XI (Accessory nerve disorder)
nerve root and plexus: Brachial plexus lesion - Thoracic outlet syndrome - Phantom limb
mononeuropathy: Carpal tunnel syndrome - Ulnar nerve entrapment - Radial neuropathy - Causalgia - Meralgia paraesthetica - Tarsal tunnel syndrome - Morton's neuroma - Mononeuritis multiplex

Polyneuropathies
and other disorders of the PNS

Hereditary and idiopathic (Charcot-Marie-Tooth disease, Dejerine Sottas syndrome, Refsum's disease, Morvan's syndrome) - Guillain-Barré syndrome - Alcoholic polyneuropathy - Neuropathy

Diseases of myoneural junction
and muscle

Myasthenia gravis - Primary disorders of muscles (Muscular dystrophy, Myotonic dystrophy, Myotonia congenita, Thomsen disease, Neuromyotonia, Paramyotonia congenita, Centronuclear myopathy, Nemaline myopathy, Mitochondrial myopathy) - Myopathy - Periodic paralysis (Hypokalemic, Hyperkalemic) - Lambert-Eaton myasthenic syndrome

Autonomic

Familial dysautonomia - Horner's syndrome - Multiple system atrophy (Shy-Drager syndrome, Olivopontocerebellar atrophy)

[[Category:Neurology


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