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Myoclonic cerebellar coordination disorder

Dysdynergia cerebellaris myoclonica was first described by Ramsay Hunt (1921), so it is also called Ramsay Hunt syndrome (RHS). However, the clinical, pathological and etiological factors of many cases reported by RHS in the future are very inconsistent. This disease is autosomal recessive inheritance. It is classified into spinocerebellar hereditary ataxia according to its gene transmission form, and its etiology is unknown.

Symptoms

Basal ganglia calcification

Acute transverse myelitis

Acute suppurative myelitis

Acute suppurative meningitis

Acute necrotizing hemorrhagic encephalomyelitis

Intraspinal hemorrhage

intramedullary abscess

Acute total autonomic nervous disorder

Anterior spinal artery syndrome

Subacute combined degeneration of spinal cord

Acute toxic encephalitis

Spinal cord ischemia

Arachnoiditis of spinal cord

Meningocele and myelomeningocele

Spinal cord schwannoma

Spinal cord injury

Spinal radiculopathy

Secondary adhesive arachnoiditis

California encephalitis

Spinal muscular atrophy

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