Diagnosing Periodic Paralysis (PP) can sometimes be a long and complicated process, with many twists and turns. The resources below may help guide you through the process. Remember to share any symptoms and testing results with your healthcare provider(s), who can work with you to find the answers you need.
Genetic Testing
Genetic Testing can be very helpful in shortening that journey. It is estimated that 80% of genetic variants (mutations) are currently known. A negative genetic test on its own may not be enough to rule out a PP. Diagnosis from a qualified physician can come in the form of genetic or clinical findings. Please discuss all symptoms and genetic testing results with your medical provider.
Other Testing
If a known genetic mutation for Periodic Paralysis is not identified, your health care provider may recommend additional testing to help make a clinical diagnosis.