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.
Analyzing 494 genes relevant to ataxia and spastic paraplegia, our panel provides thorough insights into these complex disorders.
Results delivered within 30 business days, ensuring prompt diagnosis and treatment planning.
Employing Next-Generation Sequencing (NGS) with CNV analysis for precise and reliable testing.
Our comprehensive panel includes repeat expansion analysis for common forms of inherited ataxia caused by repeat expansion mutations.
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:
Sample Requirements:
Coverage:
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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