"Leukoencephalopathies" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Any of various diseases affecting the white matter of the central nervous system.
Descriptor ID |
D056784
|
MeSH Number(s) |
C10.228.140.695
|
Concept/Terms |
Leukoencephalopathies- Leukoencephalopathies
- White Matter Diseases
- Disease, White Matter
- Diseases, White Matter
- White Matter Disease
- Leukoencephalopathy
Childhood Ataxia with Central Nervous System Hypomyelinization- Childhood Ataxia with Central Nervous System Hypomyelinization
- Leukoencephalopathy with Vanishing White Matter
- Childhood Ataxia with Diffuse Central Nervous System Hypomyelination
- Vanishing White Matter Leukodystrophy
- Cree Leukoencephalopathy
- Cree Leukoencephalopathies
- Leukoencephalopathies, Cree
- Leukoencephalopathy, Cree
- Childhood Ataxia with Central Nervous System Hypomyelination
- CACH Syndrome
- CACH Syndromes
- Syndrome, CACH
- Syndromes, CACH
- Myelinosis Centralis Diffusa
- Centralis Diffusa, Myelinosis
- Centralis Diffusas, Myelinosis
- Diffusa, Myelinosis Centralis
- Diffusas, Myelinosis Centralis
- Myelinosis Centralis Diffusas
- CACH VWM Syndrome
- CACH VWM Syndromes
- Syndrome, CACH VWM
- Syndromes, CACH VWM
- VWM Syndrome, CACH
- VWM Syndromes, CACH
|
Below are MeSH descriptors whose meaning is more general than "Leukoencephalopathies".
Below are MeSH descriptors whose meaning is more specific than "Leukoencephalopathies".
This graph shows the total number of publications written about "Leukoencephalopathies" by people in this website by year, and whether "Leukoencephalopathies" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
---|
2011 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Leukoencephalopathies" by people in Profiles.
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Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. Brain. 2020 01 01; 143(1):94-111.
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A new CUL4B variant associated with a mild phenotype and an exceptional pattern of leukoencephalopathy. Am J Med Genet A. 2017 Oct; 173(10):2803-2807.
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Spontaneously regressing leukoencephalopathy with bilateral temporal cysts in congenital rubella infection. Pediatr Infect Dis J. 2014 Apr; 33(4):422-4.
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Cerebellar hypoplasia and brainstem thinning associated with severe white matter and basal ganglia abnormalities in a child with an mtDNA deletion. J Inherit Metab Dis. 2011 Dec; 34(6):1225-7.