Neurodevelopmental Disorders
"Neurodevelopmental 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.
These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-V).
| Descriptor ID |
D065886
|
| MeSH Number(s) |
F03.625
|
| Concept/Terms |
Neurodevelopmental Disorders- Neurodevelopmental Disorders
- Disorder, Neurodevelopmental
- Disorders, Neurodevelopmental
- Neurodevelopmental Disorder
- Disorders Usually Diagnosed in Infancy, Childhood or Adolescence
- Child Mental Disorders
- Child Mental Disorder
- Disorder, Child Mental
- Disorders, Child Mental
- Mental Disorder, Child
- Mental Disorders, Child
- Mental Disorders Diagnosed in Childhood
|
Below are MeSH descriptors whose meaning is more general than "Neurodevelopmental Disorders".
Below are MeSH descriptors whose meaning is more specific than "Neurodevelopmental Disorders".
This graph shows the total number of publications written about "Neurodevelopmental Disorders" by people in this website by year, and whether "Neurodevelopmental 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 |
|---|
| 2016 | 2 | 3 | 5 |
| 2017 | 3 | 1 | 4 |
| 2018 | 2 | 0 | 2 |
| 2019 | 3 | 0 | 3 |
| 2020 | 6 | 0 | 6 |
| 2021 | 10 | 1 | 11 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Neurodevelopmental Disorders" by people in Profiles.
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Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling. Genet Med. 2022 10; 24(10):2065-2078.
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De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability. J Med Genet. 2022 10; 59(10):965-975.
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Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin. Am J Med Genet A. 2022 01; 188(1):272-282.
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Clinical trial strategies for rare neurodevelopmental disorders: challenges and opportunities. Nat Rev Drug Discov. 2021 09; 20(9):653-654.
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Expanding the KIF4A-associated phenotype. Am J Med Genet A. 2021 12; 185(12):3728-3739.
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Considering mental health and neurodevelopmental outcomes for children born extremely preterm. Dev Med Child Neurol. 2021 08; 63(8):892.
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The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals. Genet Med. 2021 08; 23(8):1492-1497.
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Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities. Am J Hum Genet. 2021 05 06; 108(5):951-961.
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Changes in Neurodevelopmental Outcomes From Age 2 to 10 Years for Children Born Extremely Preterm. Pediatrics. 2021 05; 147(5).
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De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalus. Hum Mol Genet. 2021 02 25; 29(24):3892-3899.