"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
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MeSH Number(s) |
F03.625
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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,
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Year | Major Topic | Minor Topic | Total |
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2015 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2018 | 2 | 1 | 3 |
2020 | 2 | 0 | 2 |
2021 | 7 | 0 | 7 |
2022 | 2 | 0 | 2 |
2023 | 4 | 0 | 4 |
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Below are the most recent publications written about "Neurodevelopmental Disorders" by people in Profiles.
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The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder. Am J Hum Genet. 2023 06 01; 110(6):963-978.
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Generation of induced pluripotent stem cells from two ADHD patients and two healthy controls. Stem Cell Res. 2023 06; 69:103084.
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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant. Eur J Hum Genet. 2023 04; 31(4):461-468.
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Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain. Clin Genet. 2023 04; 103(4):484-491.
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ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model. Am J Hum Genet. 2022 08 04; 109(8):1436-1457.
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Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications. Am J Hum Genet. 2022 08 04; 109(8):1421-1435.
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The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. J Mol Med (Berl). 2021 12; 99(12):1755-1768.
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Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes. Am J Med Genet A. 2021 12; 185(12):3900-3904.
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Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies. Genet Med. 2021 11; 23(11):2138-2149.
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Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders. Am J Hum Genet. 2021 08 05; 108(8):1450-1465.