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Autosomal dominant leukodystrophy with autonomic disease

Diseases of the Nervous System

Autosomal dominant leukodystrophy with autonomic disease is a rare neurological condition of genetic origin. It is characterized by gradual demyelination of the central nervous system, the loss of the insulating myelin sheath around nerve fibers, which results in a range of impairments including ataxia, mild cognitive disability and autonomic dysfunction. The name indicates a dominant pattern of inheritance, and the condition belongs to a group of disorders called leukodystrophies, which are defined by abnormalities of the white matter of the nervous system.

Facts
Classification
Body System
Nervous System 1
Communicable or Non-communicable
Non-Communicable 1
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
First Described
1964 1
Sources
1. Autosomal dominant leukodystrophy with autonomic disease (Wikipedia)
  • Lead
    gradual demyelination of the central nervous system
  • Lead [causative-agent-category]
    rare neurological condition of genetic origin
  • Lead: disease category
    Autosomal dominant leukodystrophy with autonomic disease is a rare neurological condition of genetic origin which is characterized by gradual demyelination of the central nervous system which results in various impairments, including ataxia, mild cognitive disability and autonomic dysfunction.
  • Article text
    This condition was first discovered in 1964 by E Zerbin-Rüdin et al.
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