Autism and Genetic Testing
There is no current genetic test available to diagnose autism. The exact cause of autism is still unknown, and up to 100 genes have been found to have some link to autism, but no single one has been identified as responsible for causing it. There is also the contribution of possible environmental features to it as well. Is autism genetic, is a question that just can not be answered currently.
However a diagnosis of autism, in a child or adult, may lead to a recommendation for genetic testing. This is because autism, and autistic like behaviors, are often features of specific rare diseases.
Generally a diagnosis of autism alone might not be considered enough to pursue genetic testing, but the presence of autistic like behaviors, with other symptoms, such as unique or characteristic facial features, might be enough for a genetic counselor to recommend genetic testing.
What autistic features or autism-like behaviors might trigger genetic testing?
-A lack of social interaction with others, including family members and peers
-A lack of understanding and use of social cues
-A need for routine, and the inability to handle even minor changes to this routine
-Avoidance of physical contact
-A focused interest in specific interests or activities, including repetitive behaviors
The combination of these autistic-like features may be the symptom of a rare disease, if they also present with unique facial facials, and/or other medical and health conditions.
What rare diseases present with autism-like features?
This rare disease is also often accompanied by an autism spectrum disorder diagnosis for some individuals diagnosed with the syndrome. Symptoms vary widely however between individuals with the same diagnosis. This rare disease is caused by a mutation in the TCF4 gene, and generally the syndrome is not inherited but occurs spontaneously. Other features of the syndrome include developmental delay, intellectual impairment, and low muscle tone in infancy.
This rare disease is caused by the absence of DNA on chromosome 7. Autistic-like symptoms are very common with this syndrome and include, language delay specifically, gross motor delay, a hypersensitivity to sounds and other sensory impairments, as well as issues with food and eating related to pickiness. Williams-Beuren also presents in individuals through very distinct facial features, and health conditions affecting the cardiovascular system.
This rare disease is inherited in an X-linked pattern, and affects males much more severely than females because of this. It is estimated that anywhere between 15-20% of individuals with Fragile X also display autistic-like symptoms. These range from limited eye contact, extreme responses to sensory experiences, and speech and language delay. Other identifying features of the syndrome include a high palate, long face, low muscle tone, and flat feet.
This neurological rare disease presents with autistic-like behaviors, and affects mainly females. Individuals with the syndrome have different brain pathologies and mapping than those diagnosed with autism spectrum disorder, but some of their behaviors are the same. These behaviors include repetitive movements including body rocking, and sleep difficulties. Individuals with the syndrome experience a regression in their development, including their emotional, physical and cognitive development, as they grow older.
What should I do if I noticed autistic-like behaviors in my child?
First and foremost, speak to your doctor. They will help you understand if to pursue an autism diagnosis, or not. They may also make the decision to suggest the option of genetic counseling, especially if they also identify other possible symptoms in your child that have no apparent or clear cause.
A genetic counselor will be able to understand autistic-like features in a child and individual, within the context of a possible rare disease diagnosis, and recommend the best options for further investigation and genetic testing, if deemed relevant.
Early intervention for children with autism spectrum disorder symptoms, and at the same time ensuring families and individuals receive this crucial support should be a priority for all medical teams and professionals.