Autism Spectrum Disorder (ASD) has a strong genetic component, and
genetic testing can provide valuable insights into its underlying causes.
Genetic testing involves analysing DNA to identify mutations or variations that
may contribute to autism. Common methods include chromosomal microarray
analysis (CMA) and whole exome sequencing (WES).
Identifying genetic factors through testing can help in understanding the
biological basis of autism, aiding in early diagnosis and personalized
interventions. For families, genetic results can provide clarity about the
likelihood of ASD recurrence in future children. Additionally, knowing specific
genetic variations can inform targeted therapies and medical management,
addressing associated health issues like epilepsy or gastrointestinal problems.
While genetic testing does not diagnose autism on its own, it is a
crucial tool in the broader diagnostic and therapeutic process. Collaboration
between geneticists, healthcare providers, and families ensures that the
insights gained from genetic testing are effectively integrated into the care
and support of individuals with autism.
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https://www.mentalcare.in/
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