Hyperkalemic periodic paralysis is a disorder that involves occasional episodes of muscle weakness and, sometimes, higher than normal levels of potassium in the blood.
Periodic paralysis - hyperkalemic
Hyperkalemic periodic paralysis is congenital, which means it is present from before birth. In most cases, it is passed down through families (inherited) as an autosomal dominant disorder. That means only one parent needs to pass the gene related to this condition on to you in order for you to be affected.
Occasionally, the condition may be the result of a genetic problem that is not passed down through families.
It is believed that the disorder is related to problems with the way the body controls sodium and potassium levels in cells.
Risk factors include a family history of periodic paralysis. The condition occurs in approximately 1 in every 100,000 people. It affects men more often than women.
Symptoms include attacks of muscle weakness or loss of muscle movement (paralysis) that come and go. There is normal muscle strength between attacks.
Attacks usually begin in childhood. How often the attacks occur varies. Some people have several attacks a day. Attacks typically last only 1 to 2 hours, but can sometimes last as long as a day. They are usually not severe enough to need therapy. Some people have associated myotonia, in which they cannot immediately relax their muscles after use.
The weakness or paralysis:
Triggers may include:
The health care provider may suspect hyperkalemic periodic paralysis based on a family history of the disorder. Other clues to the disorder are muscle weakness symptoms that come and go with normal or high results of a potassium test.
Between attacks, a physical examination shows nothing abnormal. Persons with hyperkalemic periodic paralysis may have normal or high levels of potassium in the bloodstream during and between attacks.
During an attack, muscle reflexes are decreased or absent, and muscles go limp rather than staying stiff. The muscle groups near the body, such as shoulders and hips, are involved more often than the arms and legs.
The health care provider may run additional tests to rule out other causes.
The goal of treatment is to relieve symptoms and prevent further attacks.
Attacks are seldom severe enough to require emergency treatment. However, weakness can become worse with repeated attacks, so treatment to prevent the attacks should occur as soon as possible.
Glucose or other carbohydrates (sugars) given during an attack may reduce the severity of the symptoms. Calcium or diuretics, such as furosemide, may need to be given through a vein to stop sudden attacks.
Sometimes attacks disappear later in life on their own. However, repeated attacks may lead to permanent muscle weakness .
Hyperkalemic periodic paralysis responds well to treatment. Treatment may prevent, and may even reverse, progressive muscle weakness.
Call your health care provider if you have intermittent muscle weakness, particularly if there is a family history of periodic paralysis.
Go to the emergency room or call the local emergency number (such as 911) if you faint or have difficulty breathing, speaking, or swallowing. These are emergency symptoms.
A medicine called acetazolamide prevents attacks in many cases. Thiazide diuretics such as hydrochlorothiazide are also effective and have fewer side effects than acetazolamide. A low potassium, high carbohydrate diet may also help prevent attacks, as may avoiding fasting, strenuous activity, or cold temperatures.
Chinnery PF. Muscle diseases.In: Goldman L, Schafer AI, eds.Cecil Medicine. 24th ed. Philadelphia, PA: Saunders Elsevier; 2011:chap 429.