Spasms, Infantile
"Spasms, Infantile" 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.
An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
Descriptor ID |
D013036
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MeSH Number(s) |
C10.228.140.490.375.760 C10.228.140.490.493.875
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Concept/Terms |
Spasms, Infantile- Spasms, Infantile
- Infantile Spasm
- Infantile Spasms
- Lightning Attacks
- Attack, Lightning
- Attacks, Lightning
- Lightning Attack
- West Syndrome
- Syndrome, West
Jackknife Seizures- Jackknife Seizures
- Jackknife Seizure
- Seizure, Jackknife
- Seizures, Jackknife
Symptomatic Infantile Spasms- Symptomatic Infantile Spasms
- Infantile Spasm, Symptomatic
- Infantile Spasms, Symptomatic
- Spasm, Symptomatic Infantile
- Spasms, Symptomatic Infantile
- Symptomatic Infantile Spasm
- Symptomatic West Syndrome
- Syndrome, Symptomatic West
- West Syndrome, Symptomatic
Salaam Attacks- Salaam Attacks
- Attacks, Salaam
- Salaam Seizures
- Seizures, Salaam
Cryptogenic Infantile Spasms- Cryptogenic Infantile Spasms
- Cryptogenic Infantile Spasm
- Infantile Spasm, Cryptogenic
- Infantile Spasms, Cryptogenic
- Spasm, Cryptogenic Infantile
- Spasms, Cryptogenic Infantile
- Cryptogenic West Syndrome
- Syndrome, Cryptogenic West
- West Syndrome, Cryptogenic
Nodding Spasm- Nodding Spasm
- Nodding Spasms
- Spasm, Nodding
- Spasms, Nodding
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Below are MeSH descriptors whose meaning is more general than "Spasms, Infantile".
Below are MeSH descriptors whose meaning is more specific than "Spasms, Infantile".
This graph shows the total number of publications written about "Spasms, Infantile" by people in this website by year, and whether "Spasms, Infantile" 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 |
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2006 | 1 | 0 | 1 | 2010 | 1 | 0 | 1 | 2016 | 2 | 0 | 2 | 2017 | 3 | 1 | 4 | 2018 | 4 | 1 | 5 | 2019 | 6 | 2 | 8 | 2020 | 8 | 0 | 8 | 2021 | 11 | 0 | 11 | 2022 | 12 | 3 | 15 | 2023 | 8 | 2 | 10 | 2024 | 7 | 2 | 9 |
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Below are the most recent publications written about "Spasms, Infantile" by people in Profiles.
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Saldaris JM, Demarest S, Jacoby P, Olson HE, Maski K, Pestana-Knight E, Price D, Rajaraman R, Suter B, Weisenberg J, Leonard H, Marsh ED, Benke TA, Downs J. Modification of a parent-report sleep scale for individuals with CDKL5 deficiency disorder: a psychometric study. J Clin Sleep Med. 2024 Dec 01; 20(12):1887-1893.
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Haviland I, Hector RD, Swanson LC, Verran AS, Sherrill E, Frazier Z, Denny AM, Lucash J, Zhang B, Dubbs HA, Marsh ED, Weisenberg JL, Leonard H, Crippa M, Cogliati F, Russo S, Suter B, Rajaraman R, Percy AK, Schreiber JM, Demarest S, Benke TA, Chopra M, Yu TW, Olson HE. Deletions in the CDKL5 5' untranslated region lead to CDKL5 deficiency disorder. Am J Med Genet A. 2025 Jan; 197(1):e63843.
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Saldaris JM, Jacoby P, Downs J, Marsh ED, Leonard H, Pestana-Knight E, Rajaraman R, Weisenberg J, Suter B, Olson HE, Price D, Hong W, Prange E, Benke TA, Demarest S. Psychometric evaluation of clinician- and caregiver-reported clinical severity assessments for individuals with CDKL5 deficiency disorder. Epilepsia. 2024 Oct; 65(10):3064-3075.
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Gil-Nagel A, Cross JH, Devinsky O, Ceulemans B, Lagae L, Knupp K, Schoonjans AS, Ryvlin P, Thiele EA, Polega S, Lothe A, Nabbout R. Comprehensive scoping review of fenfluramine's role in managing generalized tonic-clonic seizures in developmental and epileptic encephalopathies. Epilepsia. 2024 Aug; 65(8):2186-2199.
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Downs J, Jacoby P, Specchio N, Cross H, Amin S, Bahi-Buisson N, Rajaraman R, Suter B, Devinsky O, Aimetti A, Busse G, Olson HE, Demarest S, Benke TA, Pestana-Knight E. Effects of ganaxolone on non-seizure outcomes in CDKL5 Deficiency Disorder: Double-blind placebo-controlled randomized trial. Eur J Paediatr Neurol. 2024 Jul; 51:140-146.
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Sim?es de Oliveira L, O'Leary HE, Nawaz S, Loureiro R, Davenport EC, Baxter P, Louros SR, Dando O, Perkins E, Peltier J, Trost M, Osterweil EK, Hardingham GE, Cousin MA, Chattarji S, Booker SA, Benke TA, Wyllie DJA, Kind PC. Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder. Mol Autism. 2024 06 14; 15(1):28.
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Mason JA, Juarez-Colunga E, Knupp KG. Electrographic screening for infantile epileptic spasms syndrome in a single sleep-wake cycle. Epilepsia. 2024 Jun; 65(6):1737-1743.
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Keeley J, Benson-Goldberg S, Saldaris J, Lariviere J, Leonard H, Marsh ED, Demarest ST, Benke TA, Jacoby P, Downs J. Communication of individuals with CDKL5 deficiency disorder as observed by caregivers: A descriptive qualitative study. Am J Med Genet A. 2024 07; 194(7):e63570.
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Saldaris JM, Jacoby P, Marsh ED, Suter B, Leonard H, Olson HE, Rajaraman R, Pestana-Knight E, Weisenberg J, Price D, Drummond C, Benke TA, Demarest S, Downs J. Adapting a measure of gross motor skills for individuals with CDKL5 deficiency disorder: A psychometric study. Epilepsy Res. 2024 Feb; 200:107287.
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Olson HE, Amin S, Bahi-Buisson N, Devinsky O, Marsh ED, Pestana-Knight E, Rajaraman RR, Aimetti AA, Rybak E, Kong F, Miller I, Hulihan J, Demarest S. Long-term treatment with ganaxolone for seizures associated with cyclin-dependent kinase-like 5 deficiency disorder: Two-year open-label extension follow-up. Epilepsia. 2024 Jan; 65(1):37-45.
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