Structured Summary
Abstract
Rare leukoencephalopathy with infantile-onset accumulation of Rosenthal fibers in the subpial, periventricular, and subependymal zones of the brain. Rosenthal fibers are GLIAL FIBRILLARY ACIDIC PROTEIN aggregates found in ASTROCYTES. Juvenile- and adult-onset types show progressive atrophy of the lower brainstem instead. De novo mutations in the GFAP gene are associated with the disease with propensity for paternal inheritance.
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Synonyms
6 entry terms
- Alexander's Disease
- Demyelinogenic Leukodystrophy
- Dysmyelinogenic Leukodystrophy
- Fibrinoid Degeneration of Astrocytes
- Leukodystrophy with Rosenthal Fibers
- Alexanders Disease
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2003
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AMA Style
References
- National Library of Medicine. Alexander Disease. Medical Subject Headings (MeSH). 2026. Unique ID D038261. http://id.nlm.nih.gov/mesh/2026/D038261
- Alexander Disease. In: Wikipedia. https://en.wikipedia.org/wiki/Alexander_disease
- Alexander Disease. In: Wikidata. https://www.wikidata.org/wiki/Q567820