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 Disorders- Language Development Disorders
- Development Disorder, Language
- Language Development Disorder
- Speech or Language, Developmental Disorder
- Language Disorders, Developmental
- Developmental Disorder, Speech or Language
- Developmental Language Disorders
- Developmental Language Disorder
- Language Disorder, Developmental
Speech Delay- Speech Delay
- Delay, Speech
- Delays, Speech
- Speech Delays
|
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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Language Development Disorders" by people in Profiles.
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Eidsvåg SS, Plante E, Oglivie T, Privette C, Mailend ML. Individual Versus Small Group Treatment of Morphological Errors for Children With Developmental Language Disorder. Lang Speech Hear Serv Sch. 2019 04 23; 50(2):237-252.
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Zollino M, Marangi G, Ponzi E, Orteschi D, Ricciardi S, Lattante S, Murdolo M, Battaglia D, Contaldo I, Mercuri E, Stefanini MC, Caumes R, Edery P, Rossi M, Piccione M, Corsello G, Della Monica M, Scarano F, Priolo M, Gentile M, Zampino G, Vijzelaar R, Abdulrahman O, Rauch A, Oneda B, Deardorff MA, Saitta SC, Falk MJ, Dubbs H, Zackai E. Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients. J Med Genet. 2015 Dec; 52(12):804-14.