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Zarqa’s Ataxia Panel

“Unlock the secrets of neurological disorders with Zarqa's Ataxia / Spastic Paraplegia Panel”

Overview

Our Ataxia / Spastic paraplegia panel is meticulously designed to identify genes associated with hereditary neurological disorders characterized by ataxia and spastic paraplegia. This comprehensive test covers a spectrum of conditions including spinocerebellar ataxia (dominant and recessive), cerebellar ataxia, episodic ataxia, and pontocerebellar ataxia.

Key Features:

In-depth Coverage

Analyzing 494 genes relevant to ataxia and spastic paraplegia, our panel provides thorough insights into these complex disorders.

Fast Turnaround

Results delivered within 30 business days, ensuring prompt diagnosis and treatment planning.

Cutting-edge Technology

Employing Next-Generation Sequencing (NGS) with CNV analysis for precise and reliable testing.

Specialized Analysis

Our comprehensive panel includes repeat expansion analysis for common forms of inherited ataxia caused by repeat expansion mutations.

Specialized Panels

Ataxia / Spastic Paraplegia Comprehensive Panel: Covering 494 genes, including repeat expansion analysis for comprehensive testing.

Ataxia Repeat Expansion Panel: Focused on 13 genes specifically targeting repeat expansion mutations associated with ataxia.

Common Syndromes Covered:

  • Cerebellar ataxia
  • Episodic ataxia
  • Pontocerebellar hypoplasia
  • Spinocerebellar ataxia.

 

Sample Requirements:

  • Saliva
  • Blood
  • Dried Blood Spot(DBS)

Coverage:

  • ≥99.00% ≥20x