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
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MeSH Number(s) |
C10.597.606.150.500.550 C23.888.592.604.150.500.550
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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
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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.
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Year | Major Topic | Minor Topic | Total |
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2004 | 1 | 0 | 1 |
2006 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2010 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2021 | 1 | 0 | 1 |
2022 | 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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Predictors beyond the lesion: Health and demographic factors associated with aphasia severity. Cortex. 2022 09; 154:375-389.
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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism. Am J Hum Genet. 2021 06 03; 108(6):1138-1150.
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22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndrome. Genet Med. 2014 Apr; 16(4):318-28.
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Cerebral blood flow velocity and language functioning in pediatric sickle cell disease. J Int Neuropsychol Soc. 2010 Mar; 16(2):326-34.
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Language processing deficits in sickle cell disease in young school-age children. Dev Neuropsychol. 2009; 34(1):122-36.
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Asymmetry and dyslexia. Dev Neuropsychol. 2008; 33(6):663-81.
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Development in infants with autism spectrum disorders: a prospective study. J Child Psychol Psychiatry. 2006 Jun; 47(6):629-38.
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Cerebral hemispherectomy: hospital course, seizure, developmental, language, and motor outcomes. Neurology. 2004 May 25; 62(10):1712-21.
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A comparative evaluation of adaptive behavior in children and adolescents with autism, Down syndrome, and normal development. J Autism Dev Disord. 1991 Jun; 21(2):187-96.