Friedreichs Ataxia
رنح فريدريك
Sample Type
🧪 Blood
Results In
⏱ 25-30 Days
Fasting
✅ Not Required
Parameters
📊 1
What is Friedreichs Ataxia?
This is a genetic test to help diagnose Friedreich's Ataxia, a rare inherited condition that progressively affects the nervous system. It looks for specific genetic changes that cause the disorder.
Why is this test important?
It is essential for confirming the diagnosis of Friedreich's Ataxia in individuals presenting with characteristic symptoms like progressive difficulty with coordination, balance, and speech. Early diagnosis can help in managing symptoms and planning care.
How to Prepare
No special preparation required.
Medically reviewed by Dr. Reena Bhaisare, Specialist – Clinical Pathology (DHA No. 06420338-001). Samples are analysed at Lifenity Genomic Laboratory DMCC, Jumeirah Lake Towers (JLT), Dubai, where Dr. Reena Bhaisare authenticates each report. About our laboratory and medical review
Frequently Asked Questions
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Medical Disclaimer: The information on this page is for educational purposes only and should not be considered medical advice. Always consult your physician or qualified healthcare provider for diagnosis and treatment. Test results should be interpreted by a qualified medical professional.