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Familial Periodic Paralysis


Michael Rubin

, MDCM, New York Presbyterian Hospital-Cornell Medical Center

Last full review/revision Jul 2020| Content last modified Jul 2020

Familial periodic paralysis is a rare inherited disorder that causes sudden attacks of weakness and paralysis. There are four different forms, which involve abnormalities in how electrolytes, such as sodium and potassium, are moved in and out of cells.

  • Muscles do not respond normally to stimulation, usually when the blood potassium level is too low or high.
  • Weakness is intermittent, affecting mainly the limbs, and is often brought on by exercising or eating too many or too few carbohydrates.
  • The diagnosis is based on the symptoms and a check of the potassium level in the blood.
  • Avoiding triggers that cause attacks and taking certain drugs can prevent attacks effectively.

Attacks of familial periodic paralysis occur in response to the amount of potassium in a person's blood. Potassium is an electrolyte and is necessary for the normal functioning of cells, nerves, and muscles (see Overview of Potassium's Role in the Body). During an attack of familial periodic paralysis, muscles do not respond to normal nerve impulses or even to artificial stimulation with an electronic instrument.

Familial periodic paralysis is autosomal dominant, which means only one affected parent is needed to pass the trait on to offspring.

The precise form that the disorder takes varies among different families. There are four forms:

  • Hypokalemic
  • Hyperkalemic
  • Thyrotoxic
  • Andersen-Tawil syndrome

In the hypokalemic form, the paralysis is caused by low levels of potassium in the blood (hypokalemia).

In the hyperkalemic form, the paralysis is caused by high levels of potassium in the blood (hyperkalemia).

In the thyrotoxic form, the paralysis is caused by low levels of potassium in the blood, and people also have signs of an overactive thyroid gland (hyperthyroidism).

In Andersen-Tawil syndrome, potassium levels can be high, low, or normal.

Symptoms of Familial Periodic Paralysis

During an attack of weakness, the person remains completely awake and alert. Muscles in the eye and face are not affected. Weakness may affect only certain muscles or all four limbs.

In the hypokalemic form, attacks generally first appear before age 16 but may appear during the 20s and always by age 30. The attacks last up to 24 hours. Often, the person awakens the day after vigorous exercise with an attack of weakness. The weakness may be mild and limited to certain muscle groups or may affect all four limbs. However, eating meals rich in carbohydrates (sometimes hours or even the day before), emotional or physical stress, alcohol ingestion, and exposure to cold can also cause attacks. Eating carbohydrates and exercising vigorously drive sugar into cells. Potassium moves with the sugar, and the result is lowered potassium levels in the blood and urine.

In the hyperkalemic form, attacks often begin by age 10. The attacks last 15 minutes to 1 hour. Weakness tends to be less severe than in the hypokalemic form. Fasting, rest shortly after exercise, or exercise after meals may trigger attacks. Myotonia (very stiff muscles caused by a delayed ability to relax the muscles after contracting them) is common. Myotonia of the eyelids may be the only symptom.

In the thyrotoxic form, attacks of weakness last hours to days and are usually triggered by exercise, stress, or eating foods rich in carbohydrates, similar to the hypokalemic form. People have symptoms of hyperthyroidism, such as anxiety, tremors, palpitations, and heat intolerance.

In Andersen-Tawil syndrome, attacks of weakness usually begin before age 20 and are triggered by rest after exercise. Episodes may last for days and occur monthly. People with this form may also have other disorders such as an abnormally curved spine (scoliosis), webbed fingers and toes (syndactyly), abnormally positioned fingers and toes (clinodactyly), a small chin (micrognathia), or low-set ears. Heart abnormalities may cause abnormal heart rhythms and increase the risk of sudden death.

Diagnosis of Familial Periodic Paralysis

  • Description of an attack
  • Level of potassium in the blood during an attack
  • Rarely provocative testing

A doctor’s best clue to the diagnosis of familial periodic paralysis is a person’s description of a typical attack. If possible, the doctor draws blood while an attack is in progress to check the level of potassium. If the level of potassium is abnormal, doctors usually do additional tests to be sure the abnormal level is not the result of other causes.

Rarely, a doctor may give the person drugs by vein (intravenously) that increase or decrease the level of potassium in the blood to see whether an attack results. This is called provocative testing.

Prevention and Treatment

  • Depends on the form

People with the hypokalemic form can take potassium chloride in an unsweetened solution or have it injected into a vein while an attack is in progress. Usually symptoms improve considerably within an hour. People with the hypokalemic form should also avoid meals rich in carbohydrates and salt, avoid alcohol after periods of rest, and avoid strenuous exercise. Acetazolamide, a drug that alters the blood’s acidity, may help prevent attacks.

People with the hyperkalemic form can stop a mild attack by doing light exercise and eating a carbohydrate-rich meal. If an attack is persistent, drugs (such as a thiazide diuretic or inhaled albuterol) can help lower the potassium level. If an attack is severe, doctors give calcium or insulin and glucose by vein. People can prevent attacks by eating frequent meals rich in carbohydrates and low in potassium and by avoiding fasting, strenuous activity after meals, and exposure to cold.

People with the thyrotoxic form are given potassium chloride (as in the hypokalemic form), and doctors closely monitor levels of potassium in the blood during severe attacks. To prevent attacks, doctors give people drugs to keep their thyroid gland functioning properly and beta-blockers (such as propranolol).

People with Andersen-Tawil syndrome may prevent attacks by making lifestyle changes, including tightly controlling levels of exercise or activity, and by taking acetazolamide. People may need a heart pacemaker or implantable cardioverter-defibrillator to control heart symptoms.

More Information

The following is an English-language resource that may be useful. Please note that THE MANUAL is not responsible for the content of this resource.

  • Muscular Dystrophy Association: Information on research, treatment, technology, and support for people living with a periodic paralysis

Drugs Mentioned In This Article

Generic Name Select Brand Names
potassium chloride K-TAB, KLOR-CON
Acetazolamide DIAMOX
propranolol INDERAL

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