Heredodegenerative Disorders, Nervous System
"Heredodegenerative Disorders, Nervous System" 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.
Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems.
| Descriptor ID |
D020271
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| MeSH Number(s) |
C10.574.500 C16.320.400
|
| Concept/Terms |
Heredodegenerative Disorders, Nervous System- Heredodegenerative Disorders, Nervous System
- Degenerative Hereditary Diseases, Nervous System
- Degenerative Hereditary Disorders, Nervous System
- Hereditary Diseases, Neurodegenerative
- Disease, Neurodegenerative Hereditary
- Diseases, Neurodegenerative Hereditary
- Hereditary Disease, Neurodegenerative
- Neurodegenerative Hereditary Disease
- Neurodegenerative Hereditary Diseases
- Neurodegenerative Diseases, Hereditary
- Disease, Hereditary Neurodegenerative
- Diseases, Hereditary Neurodegenerative
- Hereditary Neurodegenerative Disease
- Neurodegenerative Disease, Hereditary
- Hereditary-Degenerative Disorders, Nervous System
- Hereditary Degenerative Disorders, Nervous System
- Nervous System Degenerative Hereditary Diseases
- Nervous System Diseases, Degenerative, Hereditary
- Nervous System Hereditary Degenerative Diseases
- Degenerative Disease, Nervous System, Hereditary
- Hereditary Neurodegenerative Diseases
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Below are MeSH descriptors whose meaning is more general than "Heredodegenerative Disorders, Nervous System".
Below are MeSH descriptors whose meaning is more specific than "Heredodegenerative Disorders, Nervous System".
This graph shows the total number of publications written about "Heredodegenerative Disorders, Nervous System" by people in this website by year, and whether "Heredodegenerative Disorders, Nervous System" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 2 | 0 | 2 |
| 2020 | 2 | 0 | 2 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Heredodegenerative Disorders, Nervous System" by people in Profiles.
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Atypical Presentations of Huntington Disease-like 2 in South African Individuals. Mov Disord Clin Pract. 2024 Jul; 11(7):850-854.
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A comparison between the neurocognitive profile of Huntington Disease-Like 2 and Huntington Disease: Exploring the presence of double dissociations. Appl Neuropsychol Adult. 2022 Mar-Apr; 29(2):223-233.
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The Neuropsychiatry of Huntington Disease-Like 2: A Comparison with Huntington's Disease. J Huntingtons Dis. 2020; 9(4):325-334.
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The neuropsychological deficits and dissociations in Huntington Disease-Like 2: A series of case-control studies. Neuropsychologia. 2020 01; 136:107238.
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Emerging differences between Huntington's disease-like 2 and Huntington's disease: A comparison using MRI brain volumetry. Neuroimage Clin. 2019; 21:101666.
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A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci. J Neurol Sci. 2018 07 15; 390:200-204.
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Absence of Acanthocytosis in Huntington's Disease-like 2: A Prospective Comparison with Huntington's Disease. Tremor Other Hyperkinet Mov (N Y). 2017; 7:512.
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A Systematic Review of the Huntington Disease-Like 2 Phenotype. J Huntingtons Dis. 2017; 6(1):37-46.
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The Frequency of Huntington Disease and Huntington Disease-Like 2 in the South African Population. Neuroepidemiology. 2016; 46(3):198-202.
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Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype. Am J Med Genet B Neuropsychiatr Genet. 2015 Oct; 168(7):573-85.