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Published on: September 27, 2020
Neurodevelopmental behavioral and cognitive disorders
Insights
This review covers common neurodevelopmental disorders like ADHD and autism, detailing their diagnosis, neurobiology, and treatment. Advances in genetics and understanding brain development promise improved therapies for these lifelong conditions.
Area of Science:
- Neuroscience
- Genetics
- Developmental Psychology
Background:
- Neurodevelopmental disorders encompass conditions affecting motor, social, language, and cognitive skills.
- Commonly diagnosed disorders include ADHD, autism spectrum disorder, global developmental delay, and intellectual disability.
Observation:
- Abnormal brain maturation, preceding clinical symptoms, underlies these disorders.
- Research focuses on identifying predictive biological and behavioral markers for early intervention.
- Genetic advances, including whole exome sequencing, have identified numerous mutations and syndromes linked to abnormal brain development.
Findings:
- Genetic discoveries enhance understanding of atypical development mechanisms.
- Identification of genetic variants allows for characterization of more homogeneous subgroups.
- Challenges persist into adulthood, including managing comorbidities and providing educational/vocational support.
Implications:
- Improved understanding of neurobiology and developmental trajectories will drive treatment advances.
- Mechanism-based therapies are being developed for genetic syndromes.
- Targeted treatments may expand to nonsyndromic forms of neurodevelopmental disorders.
Purpose Of Review:
Neurodevelopmental disorders are a group of heterogeneous conditions characterized by a delay or disturbance in the acquisition of skills in a variety of developmental domains, including motor, social, language, and cognition. This article reviews the most commonly diagnosed neurodevelopmental disorders, which include attention deficit hyperactivity disorder (ADHD), autism spectrum disorder, global developmental delay, and intellectual disability and also provides updates on diagnosis, neurobiology, treatment, and issues surrounding the transition to adulthood.
Recent Findings:
Although symptoms emerge at discrete points in childhood, these disorders result from abnormal brain maturation that likely precedes clinical impairment. As a result, research has focused on the identification of predictive biological and behavioral markers, with the ultimate goal of initiating treatments that may either alter developmental trajectories or lessen clinical severity. Advances in the methods used to identify genetic variants, from chromosomal microarray analysis to whole exome sequencing, have facilitated the characterization of many genetic mutations and syndromes that share common pathways to abnormal circuit formation and brain development. Not only do genetic discoveries enrich our understanding of mechanisms underlying atypical development, but they also allow us to identify more homogeneous subgroups within this spectrum of conditions. Impairments do continue into adulthood, with challenges in the transition to adulthood including the management of comorbidities and the provision of educational and vocational supports.
Summary:
Advances in our understanding of the neurobiology and developmental trajectories of these disorders will pave the way for tremendous advances in treatment. Mechanism-based therapies for genetic syndromes are being studied with the goal of expanding targeted treatments to nonsyndromic forms of neurodevelopmental disorders.
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