"Developmental Disabilities" 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.
Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed)
- Developmental Disabilities
- Disabilities, Developmental
- Developmental Disability
- Disability, Developmental
- Development Disorders, Child
- Child Development Disorder
- Development Disorder, Child
- Child Development Disorders
Child Development Deviations
- Child Development Deviations
- Child Development Deviation
- Development Deviation, Child
- Development Deviations, Child
- Deviation, Child Development
Below are MeSH descriptors whose meaning is more general than "Developmental Disabilities".
Below are MeSH descriptors whose meaning is more specific than "Developmental Disabilities".
This graph shows the total number of publications written about "Developmental Disabilities" by people in this website by year, and whether "Developmental Disabilities" was a major or minor topic of these publications.
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|Year||Major Topic||Minor Topic||Total|
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Below are the most recent publications written about "Developmental Disabilities" by people in Profiles.
Health Equity for Individuals With Intellectual and Developmental Disabilities. JAMA. 2022 10 25; 328(16):1587-1588.
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders. Brain. 2022 09 14; 145(9):3274-3287.
Defining A High-Quality Transition for Youth With Intellectual and Developmental Disabilities. Pediatrics. 2022 07 01; 150(1).
Considering mental health and neurodevelopmental outcomes for children born extremely preterm. Dev Med Child Neurol. 2021 08; 63(8):892.
RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function. J Hum Genet. 2021 Nov; 66(11):1101-1112.
Children Treated for Nonsyndromic Craniosynostosis Exhibit Average Adaptive Behavior Skills with Only Minor Shortcomings. Plast Reconstr Surg. 2021 02 01; 147(2):453-464.
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia. Genet Med. 2021 05; 23(5):881-887.
Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor a Gene (pC380SfsX9) Mutation. Thyroid. 2021 06; 31(6):1003-1005.
Concurrent validity of the Warner Initial Developmental Evaluation of Adaptive and Functional Skills and the Bayley Scales of Infant and Toddler Development, Third Edition. Dev Med Child Neurol. 2021 03; 63(3):349-354.
Defining the phenotypical spectrum associated with variants in TUBB2A. J Med Genet. 2021 01; 58(1):33-40.