Intellectual disability is a complex condition with diverse genetic origins. Zarqa’s Intellectual Disability Panel offers a comprehensive solution, analyzing genes associated with various mechanisms of inheritance and related syndromes to provide precise diagnoses and tailored interventions.
Our panel includes genes associated with intellectual disabilities across all mechanisms of inheritance, covering syndromic and non-syndromic autism, microcephaly, neuronal migration disorders, developmental regression, and Aicardi Goutierres.
With repeat expansion analysis of FMR1, our panel enables the detection of Fragile X syndrome, a common cause of intellectual disability.
Utilizing Next-Generation Sequencing (NGS) with CNV analysis and repeat expansion analysis for accurate and reliable results.
Results delivered within 30 business days, facilitating timely diagnosis and intervention for patients.
And more…
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Discover our advanced genomic testing services tailored for your specific needs. Contact us today to enhance your research with unparalleled accuracy and expertise.
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