"Muscle Hypertonia" 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.
Abnormal increase in skeletal or smooth muscle tone. Skeletal muscle hypertonicity may be associated with PYRAMIDAL TRACT lesions or BASAL GANGLIA DISEASES.
| Descriptor ID |
D009122
|
| MeSH Number(s) |
C10.597.613.550 C23.888.592.608.550
|
| Concept/Terms |
Muscle Hypertonia- Muscle Hypertonia
- Hypertonia, Muscle
- Hypertonias, Muscle
- Muscle Hypertonias
- Muscle Tone Increased
- Increased, Muscle Tone
- Tone Increased, Muscle
- Muscular Hypertonicity
- Hypertonicities, Muscular
- Hypertonicity, Muscular
- Muscular Hypertonicities
- Hypermyotonia
- Hypermyotonias
Hypertonia, Transient- Hypertonia, Transient
- Hypertonias, Transient
- Transient Hypertonia
- Transient Hypertonias
Hypertonia, Neonatal- Hypertonia, Neonatal
- Hypertonias, Neonatal
- Neonatal Hypertonia
- Neonatal Hypertonias
Hypertonia, Sphincter- Hypertonia, Sphincter
- Hypertonias, Sphincter
- Sphincter Hypertonia
- Sphincter Hypertonias
Hypertonia, Detrusor Muscle- Hypertonia, Detrusor Muscle
- Detrusor Muscle Hypertonia
- Detrusor Muscle Hypertonias
- Hypertonias, Detrusor Muscle
- Muscle Hypertonia, Detrusor
- Muscle Hypertonias, Detrusor
Hypertonia, Infantile- Hypertonia, Infantile
- Hypertonias, Infantile
- Infantile Hypertonia
- Infantile Hypertonias
|
Below are MeSH descriptors whose meaning is more general than "Muscle Hypertonia".
Below are MeSH descriptors whose meaning is more specific than "Muscle Hypertonia".
This graph shows the total number of publications written about "Muscle Hypertonia" by people in this website by year, and whether "Muscle Hypertonia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 0 | 1 |
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Below are the most recent publications written about "Muscle Hypertonia" by people in Profiles.
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A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. J Child Neurol. 2008 Dec; 23(12):1433-8.