Periodic Paralysis Syndrome
(Familial Periodic Paralysis; Hypokalemic Periodic Paralysis; Anderson-Tawil Syndrome; Paraneoplastic Periodic Paralysis)En Español (Spanish Version)
Periodic paralysis is a rare inherited condition that causes occasional episodes of severe muscle weakness. The two most common types of periodic paralysis are hypokalemic and hyperkalemic .
Periodic paralysis is a congenital condition, meaning it is present from birth. Familial periodic paralysis is inherited but may occur without a known family history. Periodic paralysis is caused by abnormalities of the electrolyte channels on muscles.
The inherited form of the disorder is autosomal dominant, which means that only one affected parent is needed to transmit the gene to the baby. When one parent is affected, the child has a 50% chance of getting the disease. Rarely, the condition occurs as a result of a noninherited genetic defect.
© 2008 Nucleus Medical Art, Inc.
A risk factor is something that increases your chance of getting a disease or condition. Those at increased risk of having periodic paralysis are:
- Children and adolescents
- Those with a family history of periodic paralysis
- Those with thyroid disorders (particularly in Asian males)
While muscle strength returns to normal between attacks, repeated bouts of weakness may lead to chronic muscle weakness later in life. The person remains alert and aware during attacks, and there is no accompanying loss of sensation.
Episodic bouts of severe weakness in the arms and legs are the most prominent symptom. Typically these bouts occur during sleep, especially after strenuous activity. Cold, stress, and alcohol may also produce attacks. Other, less common, symptoms may include:
- Weakness in the eyelids and face muscles
- Muscle pain
- Irregular heartbeats (arrythmias)
- Difficulty breathing or swallowing (if this occurs, proceed immediately to the nearest emergency room)
Some features are specific to the type of periodic paralysis.
- Potassium levels are low during attacks
- Frequency of attacks varies from daily to yearly
- Attacks usually last between 4 to 24 hours, but can last for several days
- Attacks usually begin in adolescence, but they can occur before age 10
- Potassium levels are high during attacks
- Attacks are usually shorter (lasting 1 to 2 hours), more frequent , and less severe than the hypokalemic form; breathing and swallowing difficulties are extremely rare
- Between attacks, patients often experience muscle spasms or difficulty relaxing their muscles, a condition known as myotonia
- Attacks usually begin in early childhood
Because this primarily is an inherited condition, the most important aspect of diagnosis is obtaining a family history. In addition to asking about symptoms and your medical history, your doctor will perform a physical exam.
Attacks don’t usually occur during an office visit, so your doctor may prescribe several blood tests to check potassium levels during an attack. These tests can be performed in an emergency room or laboratory.
Your doctor may wish to bring on an attack during an office visit. This should only be done under careful monitoring by an experienced neurologist.
Giving oral glucose or glucose and subcutaneous insulin may trigger a hypokalemic attack, whereas giving potassium may trigger a hyperkalemic attack. If an attack is triggered, several tests may be administered. They include:
- Blood tests to look for the gene mutation or to look for antibodies that may cause these types of symptoms.
- Electrocardiogram (ECG) to test for abnormal activity of the heart
- Electromyography (EMG) to test the functioning of nerves and muscles
© 2008 Nucleus Medical Art, Inc.
A muscle biopsy, in which a small piece of muscle tissue is removed and then sent to the lab for analysis, may be performed if the diagnosis is in question.
Since there is no cure for periodic paralysis, lifelong treatment of periodic paralysis 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:
- Eat a low carbohydrate, low sodium diet
- Avoid strenuous exercise
- Eat a low potassium diet
- Stay warm
- Avoid fasting, alcohol, and unaccustomed heavy exercise
Both hypokalemic and hyperkalemic:
- Acetazolamide (Diamox) may prevent an attack by reducing the flow of potassium from the bloodstream into the cells of the body.
- Potassium (pill or liquid form) may stop an attack; intravenous potassium may be prescribed for severe weakness.
- Avoiding certain commonly prescribed medications may help reduce the onset of attacks.
- Treat thyroid disorder if present.
- Thiazide diuretics, or ‘water pills,’ may be prescribed to prevent an attack
- Glucose, glucose and insulin, or calcium carbonate may be prescribed to slow or stop an attack
Muscular Dystrophy Association
National Organization for Rare Disorders (NORD)
Periodic Paralysis Resource Center
Muscular Dystrophy Canada
Jurkat-Ratt K, Lehmann-Horn F. Paroxysmal muscle weakness-the periodic paralyses. Journal of Neurology . 2006;253:1391-1398.
Miller TM. Correlating phenotype and genotype in the periodic paralyses. Neurology . 2004;63(9):1647-55
National Institute of Neurological Disorders and Stroke website. Available at: http://www.ninds.nih.gov . Accessed August 2005.
Patient page: attacks of immobility caused by diet or exercise? The mystery of periodic paralyses. Neurology . 2004;63(9):E17-8.
Periodic Paralysis Association website. Available at: http://www.periodicparaysis.org . Accessed August 2005.
Last reviewed January 2008 by Rimas Lukas, 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.
Copyright © 2011 EBSCO Publishing All rights reserved.