"Hemiplegia" 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.
Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body.
| Descriptor ID |
D006429
|
| MeSH Number(s) |
C10.597.622.295 C23.888.592.636.312
|
| Concept/Terms |
Hemiplegia, Transient- Hemiplegia, Transient
- Hemiplegias, Transient
- Transient Hemiplegia
- Transient Hemiplegias
Hemiplegia, Post-Ictal- Hemiplegia, Post-Ictal
- Hemiplegia, Post Ictal
- Hemiplegias, Post-Ictal
- Post-Ictal Hemiplegia
- Post-Ictal Hemiplegias
Hemiplegia, Crossed- Hemiplegia, Crossed
- Crossed Hemiplegia
- Crossed Hemiplegias
- Hemiplegias, Crossed
Hemiplegia, Flaccid- Hemiplegia, Flaccid
- Flaccid Hemiplegia
- Flaccid Hemiplegias
- Hemiplegias, Flaccid
Hemiplegia, Infantile- Hemiplegia, Infantile
- Hemiplegias, Infantile
- Infantile Hemiplegia
- Infantile Hemiplegias
Hemiplegia, Spastic- Hemiplegia, Spastic
- Hemiplegias, Spastic
- Spastic Hemiplegia
- Spastic Hemiplegias
|
Below are MeSH descriptors whose meaning is more general than "Hemiplegia".
Below are MeSH descriptors whose meaning is more specific than "Hemiplegia".
This graph shows the total number of publications written about "Hemiplegia" by people in this website by year, and whether "Hemiplegia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemiplegia" by people in Profiles.
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Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study. Lancet Neurol. 2012 Sep; 11(9):764-73.
MeSH information
