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																		 Language Development Disorders
 
																		 
																		
																	 
																		 
																		
																	 
																			
																					
	"Language Development Disorders" 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.
 
	
	
		
			
			
				Conditions characterized by language abilities (comprehension and expression of speech and writing) that are below the expected level for a given age, generally in the absence of an intellectual impairment. These conditions may be associated with DEAFNESS; BRAIN DISEASES; MENTAL DISORDERS; or environmental factors.
    
			 
				
				
					
						| Descriptor ID | D007805 |  
						| MeSH Number(s) | C10.597.606.150.500.550 C23.888.592.604.150.500.550 |  
						| Concept/Terms | Language Development DisordersLanguage Development DisordersDevelopment Disorder, LanguageLanguage Development DisorderSpeech or Language, Developmental DisorderLanguage Disorders, DevelopmentalDevelopmental Disorder, Speech or LanguageDevelopmental Language DisordersDevelopmental Language DisorderLanguage Disorder, Developmental
 Speech DelaySpeech DelayDelay, SpeechDelays, SpeechSpeech Delays
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				Below are MeSH descriptors whose meaning is more general than "Language Development Disorders". 
				Below are MeSH descriptors whose meaning is more specific than "Language Development Disorders". 
	
	
		
			
			
					
				This graph shows the total number of publications written about "Language Development Disorders" by people in this website by year, and whether "Language Development Disorders" 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 | 
|---|
 | 2003 | 0 | 1 | 1 |  | 2004 | 0 | 1 | 1 |  | 2006 | 0 | 1 | 1 |  | 2007 | 2 | 0 | 2 |  | 2008 | 1 | 1 | 2 |  | 2009 | 1 | 0 | 1 |  | 2010 | 0 | 2 | 2 |  | 2012 | 2 | 0 | 2 |  | 2013 | 3 | 0 | 3 |  | 2014 | 1 | 0 | 1 |  | 2016 | 0 | 1 | 1 |  | 2018 | 0 | 1 | 1 |  | 2019 | 3 | 0 | 3 |  | 2020 | 1 | 0 | 1 |  | 2021 | 1 | 1 | 2 |  | 2022 | 1 | 1 | 2 |  | 2023 | 1 | 0 | 1 |  | 2024 | 1 | 1 | 2 |  | 2025 | 2 | 1 | 3 | 
 
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				Below are the most recent publications written about "Language Development Disorders" by people in Profiles. 		
					
								
								Nasseri Moghaddam Z, Reinhardt EK, Thurm A, Potter BK, Smith M, Graham C, Tiller BH, Baker SA, Bilder DA, Bogar R, Britz J, Cafferty R, Coller DP, DeGrauw TJ, Hall V, Lipshutz GS, Longo N, Mercimek-Andrews S, Miller JS, Pasquali M, Salomons GS, Schulze A, Wheaton CP, Williams KF, Young SP, Li J, Balog S, Selucky T, Stöckler-Ipsiroglu S, Wallis H. Establishing a core outcome set for creatine transporter deficiency and guanidinoacetate methyltransferase deficiency. Orphanet J Rare Dis. 2025 Aug 07; 20(1):408.
								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).
								La Valle C, Hurewitz S, Geiger M, Pawlowski K, Baumer N, Wilkinson CL. Concurrent validity in language and motor domains on the Vineland-3 and Mullen Scales of Early Learning in young children with Down syndrome. Res Dev Disabil. 2025 Apr; 159:104966.
								Furia F, Levy AM, Theunis M, Bamshad MJ, Bartos MN, Bijlsma EK, Brancati F, Cejudo L, Chong JX, De Luca C, Dean SJ, Egense A, Goel H, Guenzel AJ, H?ffmeier U, Legius E, Mancini GMS, Marcos-Alcalde I, Niclass T, Planes M, Redon S, Ros-Pardo D, Rouault K, Schot R, Schuhmann S, Shen JJ, Tao AM, Thiffault I, Van Esch H, Wentzensen IM, Barakat TS, M?ller RS, Gomez-Puertas P, Chung WK, Gardella E, T?mer Z. The phenotypic and genotypic spectrum of individuals with mono- or biallelic ANK3 variants. Clin Genet. 2024 Nov; 106(5):574-584.
								Ha T, Morgan A, Bartos MN, Beatty K, Cogn? B, Braun D, Gerber CB, Gaspar H, Kopps AM, Rieubland C, Hurst ACE, Amor DJ, Nizon M, Pasquier L, Pfundt R, Reis A, Siu VM, Tessarech M, Thompson ML, Vincent M, de Vries BBA, Walsh MB, Wechsler SB, Zweier C, Schnur RE, Guillen Sacoto MJ, Margot H, Masotto B, Palafoll MIV, Nawaz U, Voineagu I, Slavotinek A. De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay. Am J Med Genet A. 2024 07; 194(7):e63559.
								Spellun A, Harstad E, Hojlo M, Milliken A, Pawlowski K, Sideridis G, Baumer N. Cross-Sectional Analysis of Caregiver-Reported Expressive Language Profiles and Associated Covariates in Individuals with Down Syndrome. J Dev Behav Pediatr. 2024 01 01; 45(1):e63-e71.
								Boada KL, Boada R, Pennington BF, Peterson RL. Sequencing Deficits and Phonological Speech Errors, But Not Articulation Errors, Predict Later Literacy Skills. J Speech Lang Hear Res. 2022 06 08; 65(6):2081-2097.
								Tiene SF, Cranston JS, Nielsen-Saines K, Kerin T, Fuller T, Vasconcelos Z, Marschik PB, Zhang D, Pone M, Pone S, Zin A, Brickley E, Orofino D, Brasil P, Adachi K, da Costa ACC, Lopes Moreira ME. Early Predictors of Poor Neurologic Outcomes in a Prospective Cohort of Infants With Antenatal Exposure to Zika Virus. Pediatr Infect Dis J. 2022 03 01; 41(3):255-262.
								Coursimault J, Guerrot AM, Morrow MM, Schramm C, Zamora FM, Shanmugham A, Liu S, Zou F, Bilan F, Le Guyader G, Bruel AL, Denomm?-Pichon AS, Faivre L, Tran Mau-Them F, Tessarech M, Colin E, El Chehadeh S, G?rard B, Schaefer E, Cogne B, Isidor B, Nizon M, Doummar D, Valence S, H?ron D, Keren B, Mignot C, Coutton C, Devillard F, Alaix AS, Amiel J, Colleaux L, Munnich A, Poirier K, Rio M, Rondeau S, Barcia G, Callewaert B, Dheedene A, Kumps C, Vergult S, Menten B, Chung WK, Hernan R, Larson A, Nori K, Stewart S, Wheless J, Kresge C, Pletcher BA, Caumes R, Smol T, Sigaudy S, Coubes C, Helm M, Smith R, Morrison J, Wheeler PG, Kritzer A, Jouret G, Afenjar A, Deleuze JF, Olaso R, Boland A, Poitou C, Frebourg T, Houdayer C, Saugier-Veber P, Nicolas G, Lecoquierre F. MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects. Hum Genet. 2022 Jan; 141(1):65-80.
								Andrade LM, Baker Meio MD, Gomes SC, Souza JP, Figueiredo MR, Costa RP, Brasil P, Nielsen-Saines K, Brickley E, Moreira MEL. Language delay was associated with a smaller head circumference at birth in asymptomatic infants prenatally exposed to the Zika virus. Acta Paediatr. 2021 08; 110(8):2375-2381. | 
																	
																		
																			
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