 Muscle Hypotonia
"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
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| MeSH Number(s) |
C10.597.613.575 C23.888.592.608.575
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| 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
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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 UAMS Profiles 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 |
|---|
| 2021 | 0 | 1 | 1 | | 2019 | 1 | 1 | 2 | | 2018 | 1 | 0 | 1 | | 2017 | 1 | 1 | 2 | | 2016 | 1 | 1 | 2 | | 2015 | 0 | 1 | 1 | | 2014 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2004 | 0 | 1 | 1 | | 1996 | 1 | 0 | 1 | | 1992 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Muscle Hypotonia" by people in Profiles over the past ten years.
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Adams LE, Chapman A, Cormack CL, Campbell K, Ebanks AH, Annibale DJ, Hollinger LE. Emanuel syndrome and congenital diaphragmatic hernia: A systematic review. J Pediatr Surg. 2022 Sep; 57(9):24-28.
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Harada Y, Ramakrishnaiah R, Arya K, Samanta D. Extensive reversible myelopathy secondary to acute quadriventricular noncommunicating hydrocephalus. Childs Nerv Syst. 2019 11; 35(11):2023-2026.
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Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, Alaimo JT, Graham B, Harris JM, Gibson JB, Pastore M, McBride KL, Komara M, Al-Gazali L, Al Shamsi A, Fanning EA, Wierenga KJ, Scott DA, Ben-Neriah Z, Meiner V, Cassuto H, Elpeleg O, Holder JL, Burrage LC, Seaver LH, Van Maldergem L, Mahida S, Soul JS, Marlatt M, Matyakhina L, Vogt J, Gold JA, Park SM, Varghese V, Lampe AK, Kumar A, Lees M, Holder-Espinasse M, McConnell V, Bernhard B, Blair E, Harrison V, Muzny DM, Gibbs RA, Elsea SH, Posey JE, Bi W, Lalani S, Xia F, Yang Y, Eng CM, Lupski JR, Liu P. De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. Genome Med. 2019 02 28; 11(1):12.
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Wang CC, Ortiz-Gonz?lez XR, Yum SW, Gill SM, White A, Kelter E, Seaver LH, Lee S, Wiley G, Gaffney PM, Wierenga KJ, Rasband MN. ?IV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal Neuropathy. Am J Hum Genet. 2018 06 07; 102(6):1158-1168.
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Tanaka AJ, Cho MT, Willaert R, Retterer K, Zarate YA, Bosanko K, Stefans V, Oishi K, Williamson A, Wilson GN, Basinger A, Barbaro-Dieber T, Ortega L, Sorrentino S, Gabriel MK, Anderson IJ, Sacoto MJG, Schnur RE, Chung WK. De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism. Cold Spring Harb Mol Case Stud. 2017 Nov; 3(6).
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Sierakowski J, Arthur J, Wylie T. Acute Hypotonia in an Infant. J Emerg Med. 2017 Jun; 52(6):e245-e247.
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Petrovski S, K?ry S, Myers CT, Anyane-Yeboa K, Cogn? B, Bialer M, Xia F, Hemati P, Riviello J, Mehaffey M, Besnard T, Becraft E, Wadley A, Politi AR, Colombo S, Zhu X, Ren Z, Andrews I, Dudding-Byth T, Schneider AL, Wallace G, Rosen ABI, Schelley S, Enns GM, Corre P, Dalton J, Mercier S, Latypova X, Schmitt S, Guzman E, Moore C, Bier L, Heinzen EL, Karachunski P, Shur N, Grebe T, Basinger A, Nguyen JM, B?zieau S, Wierenga K, Bernstein JA, Scheffer IE, Rosenfeld JA, Mefford HC, Isidor B, Goldstein DB. Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures. Am J Hum Genet. 2016 05 05; 98(5):1001-1010.
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Schuurs-Hoeijmakers JH, Landsverk ML, Foulds N, Kukolich MK, Gavrilova RH, Greville-Heygate S, Hanson-Kahn A, Bernstein JA, Glass J, Chitayat D, Burrow TA, Husami A, Collins K, Wusik K, van der Aa N, Kooy F, Brown KT, Gadzicki D, Kini U, Alvarez S, Fern?ndez-Ja?n A, McGehee F, Selby K, Tarailo-Graovac M, Van Allen M, van Karnebeek CD, Stavropoulos DJ, Marshall CR, Merico D, Gregor A, Zweier C, Hopkin RJ, Chu YW, Chung BH, de Vries BB, Devriendt K, Hurles ME, Brunner HG. Clinical delineation of the PACS1-related syndrome--Report on 19 patients. Am J Med Genet A. 2016 Mar; 170(3):670-5.
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Lam C, Golas GA, Davids M, Huizing M, Kane MS, Krasnewich DM, Malicdan MCV, Adams DR, Markello TC, Zein WM, Gropman AL, Lodish MB, Stratakis CA, Maric I, Rosenzweig SD, Baker EH, Ferreira CR, Danylchuk NR, Kahler S, Garnica AD, Bradley Schaefer G, Boerkoel CF, Gahl WA, Wolfe LA. Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors. Mol Genet Metab. 2015 Jun-Jul; 115(2-3):128-140.
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