"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 |
|---|
| 1995 | 0 | 1 | 1 |
| 1997 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2004 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2008 | 1 | 1 | 2 |
| 2011 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Muscle Hypotonia" by people in Profiles.
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Clinical findings from the landmark MEF2C-related disorders natural history study. Mol Genet Genomic Med. 2022 06; 10(6):e1919.
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Emanuel syndrome and congenital diaphragmatic hernia: A systematic review. J Pediatr Surg. 2022 Sep; 57(9):24-28.
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Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies. J Child Neurol. 2015 Oct; 30(12):1664-8.
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Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature. Am J Med Genet A. 2011 Sep; 155A(9):2146-53.
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Finding new etiologies of mental retardation and hypotonia: X marks the spot. Dev Med Child Neurol. 2008 Feb; 50(2):104-11.
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Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant. J Child Neurol. 2008 Jan; 23(1):112-7.
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Early onset alpha-mannosidosis with slow progression in three Hispanic males. Dev Med Child Neurol. 2007 Nov; 49(11):854-7.
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X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype. J Child Neurol. 2005 Oct; 20(10):852-7.
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POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
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Epidemiology of childhood Guillain-Barr? syndrome as a cause of acute flaccid paralysis in Honduras: 1989-1999. J Child Neurol. 2003 Nov; 18(11):741-7.