"Speech 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.
Acquired or developmental conditions marked by an impaired ability to comprehend or generate spoken forms of language.
| Descriptor ID |
D013064
|
| MeSH Number(s) |
C10.597.606.150.500.800 C23.888.592.604.150.500.800
|
| Concept/Terms |
Aprosodia- Aprosodia
- Aprosodias
- Aprosodic Speech
- Speech, Aprosodic
|
Below are MeSH descriptors whose meaning is more general than "Speech Disorders".
Below are MeSH descriptors whose meaning is more specific than "Speech Disorders".
This graph shows the total number of publications written about "Speech Disorders" by people in this website by year, and whether "Speech Disorders" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Speech Disorders" by people in Profiles.
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Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1. Neurology. 2023 08 29; 101(9):e879-e891.
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Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development. Neuropediatrics. 2018 12; 49(6):379-384.
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De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment. Am J Hum Genet. 2015 Sep 03; 97(3):493-500.
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The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language. Behav Genet. 2012 Jul; 42(4):509-27.
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Floating-Harbor syndrome in two unrelated girls: mild short stature in one patient and effective growth hormone therapy in the other. Am J Med Genet. 2001 Nov 15; 104(1):47-52.
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Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndrome. Am J Med Genet. 1997 Dec 12; 73(2):210-6.
MeSH information
