A genetic test that analyses a group of genes linked to Spastic Paraplegia, usually using next-generation sequencing (NGS).
Helps confirm a suspected inherited diagnosis of Spastic Paraplegia, guides treatment and follow-up, and identifies family members who may be at risk or carriers.
Neurological symptoms such as seizures, weakness, numbness or confusion — as advised by a neurologist.
No fasting needed.
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Yes. Genetic counselling before and after testing helps you understand the results and what they mean for you and your family.
No fasting is needed. You can eat and drink normally unless your doctor has advised otherwise.
Blood sample (EDTA tube); some genetic tests also accept saliva, tissue or other samples.
Usually within 28–29 days after the sample reaches the lab. You will receive the report online.