 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 | 1 | 3 | 4 | | 2006 | 2 | 0 | 2 | | 2007 | 4 | 1 | 5 | | 2008 | 5 | 2 | 7 | | 2009 | 2 | 2 | 4 | | 2010 | 7 | 8 | 15 | | 2011 | 4 | 1 | 5 | | 2012 | 5 | 0 | 5 | | 2013 | 7 | 0 | 7 | | 2014 | 5 | 2 | 7 | | 2015 | 8 | 1 | 9 | | 2016 | 6 | 5 | 11 | | 2017 | 5 | 7 | 12 | | 2018 | 13 | 3 | 16 | | 2019 | 9 | 4 | 13 | | 2020 | 13 | 3 | 16 | | 2021 | 6 | 7 | 13 | | 2022 | 0 | 3 | 3 | | 2023 | 2 | 6 | 8 | | 2024 | 3 | 6 | 9 | | 2025 | 3 | 1 | 4 |
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Below are the most recent publications written about "Developmental Disabilities" by people in Profiles.
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Guillouet C, Agostini V, Baujat G, Cocciadiferro D, Pippucci T, Lesieur-Sebellin M, Georget M, Schatz U, Fauth C, Louie RJ, Rogers C, Davis JM, Konstantopoulou V, Mayr JA, Bouman A, Wilke M, VanNoy GE, England EM, Park KL, Brown K, Saenz M, Novelli A, Digilio MC, Mastromoro G, Rongioletti MCA, Piacentini G, Kaiyrzhanov R, Guliyeva S, Hasanova L, Shears D, Bhatnagar I, Stals K, Klaas O, Horvath J, Bouvagnet P, Witmer PD, MacCarrick G, Cisarova K, Good JM, Gorokhova S, Boute O, Smol T, Bruel AL, Patat O, Broadbent JR, Tan TY, Tan NB, Lyonnet S, Busa T, Graziano C, Amiel J, Gordon CT. Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformations. Am J Hum Genet. 2025 Apr 03; 112(4):829-845.
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Yu AP, Suarez-Balcazar Y, Errisuriz VL, Parra-Medina D, Mirza M, Zhang M, Lee PC, Zeng W, Brown-Hollie JP, Yespica Mendoza E, Brown S, Vanegas SB, Heydarian NM, Maga?a S. PODER Familiar: A Culturally Tailored Health Intervention for Latino Families of Children With Intellectual and Developmental Disabilities. J Appl Res Intellect Disabil. 2025 Mar; 38(2):e70048.
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Johnson SL, Moody EJ, Kral TV, Holst B, Dahl E, Withrow NA, Levy SE, Reynolds AM, Rosenberg CR. A multisite community-based, case-control study to examine the nutrient intake adequacy of young children with and without developmental delays and other disorders: findings from the Study to Explore Early Development (SEED). Am J Clin Nutr. 2025 Jun; 121(6):1286-1295.
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Araya P, Phillips K, Waldie K, Underwood L. Gross Motor Development in Children With Autism: Longitudinal Trajectories From the Growing Up in New?Zealand Study. Autism Res. 2025 Feb; 18(2):437-448.
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Yeo EN, Young ND, Cleveland JC, Simon TD, Vanderbilt DL, Espinoza J, Mirzaian CB, Alderete TL. High-Risk Infant Developmental Outcome Is Associated with Medical Complexity and Neighborhood Opportunity. J Pediatr. 2025 Apr; 279:114433.
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Gracie S, Deshpande P, Hollos P, De Dios K, Martin DM, Pritchard AB, Scott Schwoerer JA, Behrmann MR, Seaver LH, Brown K, Fernandez RJ, Larson A, Coffey E. Expanding the Molecular and Clinical Phenotype of Patients With De Novo Variants in KIF5C: A Six Patient Case Series. Am J Med Genet A. 2025 Mar; 197(3):e63927.
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Baumer N, DePillis R, Pawlowski K, Zhang B, Mazumdar M. Developmental Milestones for Children With Down Syndrome. Pediatrics. 2024 Oct 01; 154(4).
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Sidpra J, Sudhakar S, Biswas A, Massey F, Turchetti V, Lau T, Cook E, Alvi JR, Elbendary HM, Jewell JL, Riva A, Orsini A, Vignoli A, Federico Z, Rosenblum J, Schoonjans AS, de Wachter M, Delgado Alvarez I, Felipe-Ruci?n A, Haridy NA, Haider S, Zaman M, Banu S, Anwaar N, Rahman F, Maqbool S, Yadav R, Salpietro V, Maroofian R, Patel R, Radhakrishnan R, Prabhu SP, Lichtenbelt K, Stewart H, Murakami Y, L?bel U, D'Arco F, Wakeling E, Jones W, Hay E, Bhate S, Jacques TS, Mirsky DM, Whitehead MT, Zaki MS, Sultan T, Striano P, Jansen AC, Lequin M, de Vries LS, Severino M, Edmondson AC, Menzies L, Campeau PM, Houlden H, McTague A, Efthymiou S, Mankad K. The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders. Brain. 2024 Aug 01; 147(8):2775-2790.
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Karayol R, Borroto MC, Haghshenas S, Namasivayam A, Reilly J, Levy MA, Relator R, Kerkhof J, McConkey H, Shvedunova M, Petersen AK, Magnussen K, Zweier C, Vasileiou G, Reis A, Savatt JM, Mulligan MR, Bicknell LS, Poke G, Abu-El-Haija A, Duis J, Hannig V, Srivastava S, Barkoudah E, Hauser NS, van den Born M, Hamiel U, Henig N, Baris Feldman H, McKee S, Krapels IPC, Lei Y, Todorova A, Yordanova R, Atemin S, Rogac M, McConnell V, Chassevent A, Bara?ano KW, Shashi V, Sullivan JA, Peron A, Iascone M, Canevini MP, Friedman J, Reyes IA, Kierstein J, Shen JJ, Ahmed FN, Mao X, Almoguera B, Blanco-Kelly F, Platzer K, Treu AB, Quilichini J, Bourgois A, Chatron N, Januel L, Rougeot C, Carere DA, Monaghan KG, Rousseau J, Myers KA, Sadikovic B, Akhtar A, Campeau PM. MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature. Am J Hum Genet. 2024 07 11; 111(7):1330-1351.
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Luehring MC, Romani PW, Ariefdjohan M. Preliminary evaluation of behavior technician burnout when working with boarded and traditional psychiatric inpatients diagnosed with developmental disabilities. J Child Adolesc Psychiatr Nurs. 2024 May; 37(2):e12461.
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