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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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 0 | 1 | 1 |
| 2001 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 2 | 1 | 3 |
| 2019 | 0 | 1 | 1 |
| 2020 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 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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Diagnosis of autism in a rare case of tyrosine hydroxylase deficiency: a case report. BMC Med Genomics. 2023 04 11; 16(1):78.
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Use and Perceived Effectiveness of Communication Modes Reported by Persons With Primary Progressive Aphasia. Am J Speech Lang Pathol. 2023 01 11; 32(1):298-305.
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Automated Phenotyping Tool for Identifying Developmental Language Disorder Cases in Health Systems Data (APT-DLD): A New Research Algorithm for Deployment in Large-Scale Electronic Health Record Systems. J Speech Lang Hear Res. 2020 09 15; 63(9):3019-3035.
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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
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Safety of Electroconvulsive Therapy in 2 Very Young Pediatric Patients With Catatonia Related to Anti-N-methyl-D-aspartate Receptor Encephalitis. J ECT. 2019 09; 35(3):216-217.
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Neurocognitive function of 10-year-old multiples born less than 28 weeks of gestational age. J Perinatol. 2019 02; 39(2):237-247.
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Cognitive Development and Quality of Life Associated With BPD in 10-Year-Olds Born Preterm. Pediatrics. 2018 06; 141(6).
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The Test of Infant Motor Performance at 3 months predicts language, cognitive, and motor outcomes in infants born preterm at 2 years of age. Dev Med Child Neurol. 2018 12; 60(12):1239-1243.
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Comparison of brain MRI findings with language and motor function in the dystroglycanopathies. Neurology. 2017 Feb 14; 88(7):623-629.
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Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay. Am J Med Genet A. 2015 Jun; 167(6):1414-7.