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Autism Spectrum Disorders Panel

(4 Customer Reviews)
$0.00

Is a 75 gene panel that includes assessment of non-coding variants.

In addition, it also includes the maternally inherited mitochondrial genome.
Is ideal for patients with clinical diagnosis of autism.Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social communication, absence or delay in language development, and stereotyped or repetitive behaviors. Autism has many etiologies, as it has been documented in hundreds of neurologically based syndromes with multiple causes, outcomes, and treatment responses. Currently a genetic cause can be identified in 20% to 25% of children with autism. Single-gene disorders, in which neurologic findings are associated with autism spectrum disorder (ASD), can be identified in ~5% of ASD patients.

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Is a 75 gene panel that includes assessment of non-coding variants.

In addition, it also includes the maternally inherited mitochondrial genome.
Is ideal for patients with clinical diagnosis of autism.Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social communication, absence or delay in language development, and stereotyped or repetitive behaviors. Autism has many etiologies, as it has been documented in hundreds of neurologically based syndromes with multiple causes, outcomes, and treatment responses. Currently a genetic cause can be identified in 20% to 25% of children with autism. Single-gene disorders, in which neurologic findings are associated with autism spectrum disorder (ASD), can be identified in ~5% of ASD patients.

Test Duration: N/A

Home Sample Collection: No

Category: Cognition & Neurology Testing

Lab: N/A

Price: $0.00

Test Features

Genetic factors can contribute to a wide range of neurological and neurodevelopmental conditions. Our Neurological Genetics Panel helps identify inherited genetic variants associated with dementia, movement disorders, neurodevelopmental conditions, and other neurological diseases, providing valuable information for diagnosis, risk assessment, family planning, and clinical management.

Our comprehensive testing panels may include genetic causes associated with: ●Alzheimer's Disease and other forms of dementia ●Frontotemporal Dementia (FTD) ●Parkinson's Disease ●Huntington's Disease ●Amyotrophic Lateral Sclerosis (ALS) ●Hereditary Ataxias ●Epilepsy and seizure disorders ●Autism Spectrum Disorder (ASD) ●Intellectual and developmental disabilities ●Other inherited neurological conditions

●Individuals with symptoms suggestive of a neurological disorder ●Those with a family history of dementia, Parkinson's disease, or other neurological conditions ●Families seeking to understand inherited risks ●Individuals considering predictive or presymptomatic testing ●Parents investigating potential genetic causes of neurodevelopmental conditions

●Supports accurate diagnosis and clinical management ●Identifies inherited risk factors ●Assists with family planning decisions ●Helps inform treatment and surveillance strategies ●Provides clarity for patients and their families

Using a blood or saliva sample, advanced genetic sequencing technology analyses genes associated with neurological and neurodevelopmental conditions. Results are interpreted by experienced specialists and may be accompanied by genetic counselling to help you understand the findings and available options. Understanding your genetics can provide valuable answers, guide healthcare decisions, and help families plan for the future with greater confidence.

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