"Muscle Hypotonia" 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.
A diminution of the skeletal muscle tone marked by a diminished resistance to passive stretching.
| Descriptor ID |
D009123
|
| MeSH Number(s) |
C10.597.613.575 C23.888.592.608.575
|
| Concept/Terms |
Muscle Hypotonia- Muscle Hypotonia
- Hypotonia, Muscle
- Decreased Muscle Tone
- Muscle Tone, Decreased
- Muscle Tone Poor
- Tone Poor, Muscle
- Hypotonia
- Hypotony, Muscle
- Muscle Hypotony
- Muscular Hypotonia
- Hypotonia, Muscular
- Hypomyotonia
Neonatal Hypotonia- Neonatal Hypotonia
- Hypotonia, Neonatal
- Hypotonias, Neonatal
- Neonatal Hypotonias
Flaccid Muscle Tone- Flaccid Muscle Tone
- Muscle Tone, Flaccid
- Muscular Flaccidity
- Flaccidity, Muscular
- Muscular Flaccidities
- Muscle Flaccidity
- Flaccidity, Muscle
Floppy Muscles- Floppy Muscles
- Floppy Muscle
- Muscle, Floppy
- Muscles, Floppy
|
Below are MeSH descriptors whose meaning is more general than "Muscle Hypotonia".
Below are MeSH descriptors whose meaning is more specific than "Muscle Hypotonia".
This graph shows the total number of publications written about "Muscle Hypotonia" by people in this website by year, and whether "Muscle Hypotonia" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 2010 | 0 | 2 | 2 |
| 2011 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 2 | 0 | 2 |
| 2019 | 1 | 0 | 1 |
| 2020 | 2 | 0 | 2 |
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click here.
Below are the most recent publications written about "Muscle Hypotonia" by people in Profiles.
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Homozygosity mapping and whole exome sequencing provide exact diagnosis of Cohen syndrome in a Saudi family. Brain Dev. 2020 Sep; 42(8):587-593.
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Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities. Am J Hum Genet. 2020 02 06; 106(2):246-255.
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A novel homozygous splice-site mutation in the SPTBN4 gene causes axonal neuropathy without intellectual disability. Eur J Med Genet. 2020 Apr; 63(4):103826.
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Microangiopathy and mild mixed neuromyopathic alterations in a patient with homozygous PIEZO-2 mutation. Neuromuscul Disord. 2018 12; 28(12):1006-1011.
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Isolated PREPL deficiency associated with congenital myasthenic syndrome-22. Klin Padiatr. 2018 09; 230(5):281-283.
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Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability. Hum Genet. 2017 07; 136(7):821-834.
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Five patients with novel overlapping interstitial deletions in 8q22.2q22.3. Am J Med Genet A. 2011 Aug; 155A(8):1857-64.
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Cohen syndrome diagnosis using whole genome arrays. J Med Genet. 2011 Feb; 48(2):136-40.
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Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Gouti?res syndrome. Arthritis Rheum. 2010 May; 62(5):1469-77.
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Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndrome. Clin Genet. 1996 Feb; 49(2):98-102.
MeSH information
