 Developmental Disabilities
"Developmental Disabilities" 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.
Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed)
| Descriptor ID |
D002658
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| MeSH Number(s) |
F03.625.421
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| Concept/Terms |
Developmental Disabilities- Developmental Disabilities
- Disabilities, Developmental
- Developmental Disability
- Disability, Developmental
- Development Disorders, Child
- Child Development Disorder
- Development Disorder, Child
- Child Development Disorders
Child Development Deviations- Child Development Deviations
- Child Development Deviation
- Development Deviation, Child
- Development Deviations, Child
- Deviation, Child Development
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Below are MeSH descriptors whose meaning is more general than "Developmental Disabilities".
Below are MeSH descriptors whose meaning is more specific than "Developmental Disabilities".
This graph shows the total number of publications written about "Developmental Disabilities" by people in this website by year, and whether "Developmental Disabilities" 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 |
|---|
| 1998 | 1 | 0 | 1 | | 2002 | 1 | 1 | 2 | | 2003 | 1 | 0 | 1 | | 2004 | 0 | 1 | 1 | | 2005 | 0 | 3 | 3 | | 2006 | 2 | 1 | 3 | | 2007 | 2 | 1 | 3 | | 2008 | 4 | 2 | 6 | | 2009 | 2 | 2 | 4 | | 2010 | 5 | 9 | 14 | | 2011 | 7 | 1 | 8 | | 2012 | 4 | 0 | 4 | | 2013 | 6 | 1 | 7 | | 2014 | 5 | 4 | 9 | | 2015 | 8 | 1 | 9 | | 2016 | 7 | 5 | 12 | | 2017 | 6 | 5 | 11 | | 2018 | 13 | 4 | 17 | | 2019 | 12 | 3 | 15 | | 2020 | 14 | 3 | 17 | | 2021 | 6 | 8 | 14 | | 2022 | 0 | 4 | 4 | | 2023 | 3 | 6 | 9 | | 2024 | 7 | 6 | 13 | | 2025 | 12 | 2 | 14 | | 2026 | 1 | 1 | 2 |
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Below are the most recent publications written about "Developmental Disabilities" by people in Profiles.
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Murthy H, Hoang N, Stark JC, Cui S, Pannia E, Tsoi CT, Harris S, Ceolin C, Verhaeghe L, Scholten S, Baribeau D, Summers J, Costain G, Selvanayagam T, Howe JL, Lewis MES, Brunet T, Rieger S, Rosenfeld JA, Craigen WJ, Burrage LC, Christie MR, Baldwin D, Wentzensen IM, Keren B, Cogne B, Isidor B, Afenjar A, Elshafie RM, Bastaki L, Alkanderi S, Myers KA, Demarest S, Angione K, Abbott M, Campeau PM, Dowling JJ, Mendoza-Londono R, Scherer SW, Deshwar AR, Vorstman J. Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia. Brain. 2026 Jan 08; 149(1):252-261.
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Thompson T, Bothwell S, Janusz J, Wilson R, Howell S, Davis S, Swenson K, Martin S, Kowal K, Ikomi C, Despradel M, Ross J, Tartaglia N. Quantifying the Spectrum of Early Motor and Language Milestones in Sex Chromosome Trisomy. Obstet Gynecol Surv. 2026 Jan 01; 81(1):12-14.
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Hayeems RZ, Ungar WJ, Marshall CR, Gillespie MK, Szuto A, Huang L, Venkataramanan V, Xiao B, Chisholm C, Stavropoulos DJ, Bergeron MB, Lee W, Costain G, Jobling R, Sawyer S, Price EM, Lau L, Mendoza R, Somerville MJ, Boycott KM. Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trial. Genet Med. 2026 Jan; 28(1):101605.
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Wiggins LD, DiGuiseppi C, Overwyk K, Barger B, Dichter G, Durkin M, Hightshoe K, Moody E, Nadler C, Powell P, Reyes N, Thompson-Paul AM, Anderson KN. Adverse Childhood Experiences and Behavioral and Emotional Problems in Adolescents With and Without Autism. J Dev Behav Pediatr. 2025 Nov-Dec 01; 46(6):e579-e585.
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Abbott M, Angione K, Stringfellow M, Malik K, Saenz M, McCourt E, Silveira L, Miele A, Benke TA, Demarest S. Cortical Visual Impairment Across a Range of Neurodevelopmental Disorders: Clinical Characterization, Diagnostic Tool Evaluation, and Association with Developmental Outcomes. J Child Neurol. 2026 Apr; 41(4):470-477.
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Thompson T, Bothwell S, Janusz J, Wilson R, Howell S, Davis S, Swenson K, Martin S, Kowal K, Ikomi C, Despradel M, Ross J, Tartaglia N. Quantifying the Spectrum of Early Motor and Language Milestones in Sex Chromosome Trisomy. Pediatrics. 2025 Aug 01; 156(2).
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Goad BS, Rodda J, Allen M, Bamborschke D, Overmars I, Kerr RJ, Bushlin I, Chopra S, Coorg R, Dabscheck G, Freeman JL, Mackay MT, Devinsky O, Guerrini R, Parrini E, Bölsterli B, Hughes I, Huh LL, Kamate M, Kunz AB, Melikishvili G, Miteff C, Myers KA, Olson HE, Poduri A, Pillai S, Riney CK, Sinclair A, Calvert S, Reynolds TQ, Martinez AR, Russo A, Sadleir LG, Sanchez-Albisua I, Sartori S, Shea S, Smith-Hicks CL, Spooner CG, Thomas RH, Ardern-Holmes SL, Webster RI, Valeriani M, Veggiotti P, Masnada S, Ware TL, Yoong M, Berecki G, De Dominicis A, Specchio N, Trivisano M, Møller RS, Wolff M, Fazeli W, Scheffer I, Howell KB. Development and Adaptive Function in Individuals With SCN2A-Related Disorders. Neurology. 2025 Aug 12; 105(3):e213868.
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Cuillerier A, Goodman A, Lawrence C, Villeneuve-Cloutier N, Armour CM, Bhola PT, Bourque DK, Carter MT, Lazier J, Sawyer SL, Saleh M, Prasad C, Siu VM, Boycott KM, Hartley T, Dyment DA, Balci TB. Diagnostic Utility of Exome Data Reanalysis After In Silico Multi-Gene Panels or Clinical Exome Testing for Patients With Epilepsy and Developmental Delay/Intellectual Disability: A Retrospective Cohort Study. Clin Genet. 2026 Jan; 109(1):40-49.
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Malthaner LQ, McLeigh JD, Knell G, Jetelina KK, Atem F, Messiah SE. Prenatal Substance Exposure and Positive Developmental Delay Screening Among Patients in Foster Care. J Dev Behav Pediatr. 2025 Jun 19; 46(4):e368-e374.
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Strong A, McKenna C, Stals K, Vitobello A, Renaud M, Rieubland C, Guipponi M, Philippe C, Vrana P, Gaskell A, Innes AM, Rippert AL, Ahrens-Nicklas R, Bhoj E, Keller K, Chaudhari BP, Stone BS. Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay. Am J Med Genet A. 2025 Oct; 197(10):e64119.
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