Periodic paralysis is a rare condition that is usually inherited. It causes occasional episodes of severe muscle weakness. The 2 most common types of periodic paralysis are hypokalemic and hyperkalemic.
Periodic paralysis is a condition that is present from birth. Periodic paralysis is caused by abnormalities of the electrolyte channels on muscles.
Familial periodic paralysis is inherited, but may occur without a known family history. With the inherited form of the disorder, only 1 affected parent is needed to transmit the gene to the baby. Rarely, the condition occurs as a result of a noninherited genetic defect.
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Factors that increase your chance of developing periodic paralysis include:
Although muscle strength returns to normal between attacks, repeated episodes of weakness may lead to chronic muscle weakness later in life. The person remains alert and aware during attacks. There is no loss of sensation.
Episodes of severe weakness in the arms and legs are the major symptom. Typically, these episodes occur during sleep, early morning, or after strenuous activity. Cold, stress, and alcohol may also produce attacks. Other, less common, symptoms may include:
Some features are specific to the type of periodic paralysis.
Persons with some types of periodic paralysis are at risk for a condition known as malignant hyperthermia. This can occur during the use of general anesthesia . Anyone with a family history of periodic paralysis needs to notify the anesthesiologist of this history prior to any surgery.
Because this primarily is an inherited condition, the most important part of diagnosis is obtaining a family history. You will be asked about your symptoms and your medical history. A physical exam will be done.
Your doctor may want to bring on an attack during an office visit. This should only be done under careful monitoring by an experienced neurologist. If an attack is triggered, several tests may be done, including:
Your muscle tissue may need to be tested. This can be done with a biopsy .
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Since there is no cure for periodic paralysis, lifelong treatment is usually required. Treatment focuses on preventing attacks and relieving symptoms.
There are a few behaviors you can adopt to reduce the frequency and severity of attacks:
The type of medications prescribed depend on the type of periodic paralysis.
Familial periodic paralysis cannot be prevented. Because it can be inherited, genetic counseling may be advised for couples at risk of passing on the disorder.
For the hypokalemic type, attacks may be reduced by:
For the hyperkalemic type, attacks may be reduced by:
Muscular Dystrophy Association
National Organization for Rare Disorders
Hyperkalemic periodic paralysis. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed. Updated April 30, 2013. Accessed June 22, 2015.
Jurkat-Ratt K, Lehmann-Horn F. Paroxysmal muscle weakness-the periodic paralyses. J Neurol. 2006;253:1391-1398.
Jurkatt-Rott K, Lerche H, Weber Y, Lehmann-Horn F. Hereditary channelopathies in neurology. Adv Exp Med Biol. 2010;686:305-334.
Miller TM. Correlating phenotype and genotype in the periodic paralyses. Neurology. 2004;63:1647-1655
NINDS familial periodic paralyses information page. National Institute of Neurological Disorders and Stroke website. Available at: http://www.ninds.nih.gov/disorders/periodic_paralysis/periodic_paralysis.htm. Updated March 12, 2012. Accessed June 22, 2015.
Patient page: attacks of immobility caused by diet or exercise? The mystery of periodic paralyses. Neurology. 2004;63:E17-E18.
Last reviewed June 2015 by Rimas Lukas, MD; Michael Woods, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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