Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Apr;43(2):465-75.
doi: 10.1093/ije/dyu037. Epub 2014 Mar 11.

Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders

Affiliations
Review

Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders

Young Shin Kim et al. Int J Epidemiol. 2014 Apr.

Abstract

Recent advances in the genetics of neurodevelopmental disorder (NDD) have demonstrated that rare mutations play a role not only in Mendelian syndromes, but in complex, common forms of NDDs as well. Strikingly, both common polymorphisms and rare variations in a single gene or genetic locus have been found to carry risk for conditions previously considered to be clinically and aetiologically distinct. Recent developments in the methods and tools available for studying complex NDDs have led to systematic and reliable genome-wide variant discovery. Both common as well as rare, and structural as well as sequence, genetic variations have been identified as contributing to NDDs. There are multiple examples in which the identical variant had been found to contribute to a wide range of formerly distinct diagnoses, including autism, schizophrenia, epilepsy, intellectual disability and language disorders. These include variations in chromosomal structure at 16p11.2, rare de novo point mutations at the gene SCN2A, and common single nucleotide polymorphisms (SNPs) mapping near loci encoding the genes ITIH3, AS3MT, CACNA1C and CACNB2. These selected examples point to the challenges to current diagnostic approaches. Widely used categorical schema have been adequate to provide an entré into molecular mechanisms of NDDs, but there is a need to develop an alternative, more biologically-relevant nosology. Thus recent advances in gene discovery in the area of NDDs are leading to a re-conceptualization of diagnostic boundaries. Findings suggest that epidemiological samples may provide important new insights into the genetics and diagnosis of NDDs and that other areas of medicine may provide useful models for developing a new diagnostic nosology, one that simultaneously integrates categorical diagnoses, biomarkers and dimensional variables.

Keywords: genetics; genomics and etiology; neurodevelopmental disorders; nosology.

PubMed Disclaimer

References

    1. Yeargin-Allsopp M, Boyle C. Overview: the epidemiology of neurodevelopmental disorders. Ment Retard Dev Disabil Res Rev 2002;8:113–16 - PubMed
    1. Accardo PJ, Capute AJ. Capute & Accardo's Neurodevelopmental Disabilities in Infancy and Childhood: Neurodevelopmental diagnosis and treatment . Baltimore, MD: Paul H Brookes, 2008
    1. American Psychiatric Association. DSM-IV. Arlington, VA: American Psychiatric Association, 1994
    1. McKusick-Nathans Institute of Genetic Medicine. Online Mendelian Inheritance in Man. Baltimore, MD: Johns Hopkins University School of Medicine, 2013
    1. Moss J, Howlin P. Autism spectrum disorders in genetic syndromes: implications for diagnosis, intervention and understanding the wider autism spectrum disorder population. J Intellect Disabil Res 2009;53:852–73 - PubMed

Publication types

Substances