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.
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Communicable or Non-communicable Causative Agent
Causative Agent (category) First Described Sources
1. Autosomal dominant leukodystrophy with autonomic disease (Wikipedia)
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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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