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Zarqa’s Intellectual Disabilty Panel

"Discover the genetic insights needed for personalized care with Zarqa's Intellectual Disability Panel."


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.

Key Features:

Comprehensive Coverage

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.

Detection of Fragile X Syndrome

With repeat expansion analysis of FMR1, our panel enables the detection of Fragile X syndrome, a common cause of intellectual disability.

Cutting-edge Technology

Utilizing Next-Generation Sequencing (NGS) with CNV analysis and repeat expansion analysis for accurate and reliable results.

Fast Turnaround

Results delivered within 30 business days, facilitating timely diagnosis and intervention for patients.

Common Syndromes Covered

  • Aicardi-Goutieres syndrome
  • Bardet-Biedl syndrome
  • Epileptic encephalopathy
  • Intellectual disability (AD, AR, XL)
  • Micro syndrome
  • Microcephaly
  • Neurodevelopmental disorders
  • Neuronal migration disorders
  • Syndromic autism

And more…

Sample Requirements:

  • Blood
  • Saliva
  • DBS



  • ≥99.00% ≥20x