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Neurodegenerative disease
Articles
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amyotrophic lateral sclerosis
23 September 2003 -
Parkinson disease
29 September 2003Parkinson’s disease, pakinsonism
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multiple system atrophy
14 April 2009While the designation multiple system atrophy (MSA) originally applied to a wide spectrum of neurodegenerative disorders affecting multiple neural "systems," it is now used to describe a group of disorders characterized by the presence of glial cytoplasmic inclusions (GCIs), typically within the cytoplasm of oligodendrocytes.
With recognition of GCIs, the three clinicopathologic entities of striatonigral degeneration, Shy-Drager syndrome, and olivopontocerebellar atrophy were gathered into (...) -
ataxia telangiectasia
27 October 2003Definition: Ataxia telangiectasia (AT) is another autosomal recessive disorder characterized by cerebellar ataxia, progressive mental retardation, immune defects, severe muscular incoordination, and a strong predisposition to malignancy, particularly in the lymphoreticular system. The term telangiectasia describes the dilatation of blood vessels, particularly in the eyes and skin.
Patients with this disease have several defects, including hypersensitivity to ionising radiation. Death is (...) -
bulbospinal atrophy
14 April 2009Kennedy syndrome
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Leigh syndrome
28 May 2003Leigh’s syndrome
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Pelizaeus-Merzbacher disease
28 October 2003Pelizaeus-Merzbacher Disease is an X-linked, invariably fatal, leukodystrophy beginning either in early childhood or just after birth, and characterized by slowly progressive signs and symptoms resulting from widespread white matter dysfunction.
Patients present with pendular eye movements, hypotonia, choreoathetosis, and pyramidal signs early in the disease, followed later by spasticity, dementia, and ataxia.
The disease has been shown to arise in most cases from defects in a gene on the (...) -
Alzheimer disease
20 October 2003Alzheimer’s disease