"Neuroacanthocytosis" 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.
An inherited autosomal disorder that is characterized by neurodegeneration; orofacial and buccal DYSKINESIAS; CHOREA; and thorny-looking red cells (ACANTHOCYTES). This disorder is due to mutations of chorein which is important in protein trafficking and is encoded by Vps13a on chromosome 9q21.
| Descriptor ID |
D054546
|
| MeSH Number(s) |
C10.228.662.262.249.937 C16.320.400.550
|
| Concept/Terms |
Neuroacanthocytosis- Neuroacanthocytosis
- Chorea Acanthocytosis Syndrome
- Chorea Acanthocytosis Syndromes
- Acanthocytosis with Neurologic Disorder
- Choreoacanthocytosis
- Choreoacanthocytoses
- Levine-Critchley Syndrome
- Levine Critchley Syndrome
- Chorea Acanthocytosis
- Acanthocytoses, Chorea
- Acanthocytosis, Chorea
- Chorea Acanthocytoses
- Chorea-Acanthocytosis
- Chorea-Acanthocytoses
|
Below are MeSH descriptors whose meaning is more general than "Neuroacanthocytosis".
Below are MeSH descriptors whose meaning is more specific than "Neuroacanthocytosis".
This graph shows the total number of publications written about "Neuroacanthocytosis" by people in this website by year, and whether "Neuroacanthocytosis" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 0 | 1 | 1 |
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Below are the most recent publications written about "Neuroacanthocytosis" by people in Profiles.
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Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders. Neurobiol Aging. 2013 Oct; 34(10):2442.e11-7.