Published:
|
|
The two most common types of periodic paralyses are:
Hypokalemic periodic paralysis is characterized by a fall in potassium levels in the blood. In individuals with this mutation attacks
often begin in adolescence and are triggered by strenuous exercise or high carbohydrate meals. Weakness may be mild and limited
to certain muscle groups, or more severe and affect the arms and legs. Attacks may last for a few hours or persist for several
days. Some patients may develop chronic muscle weakness later in life.
Hyperkalemic periodic paralysis is characterized by a rise in potassium levels in the blood. Attacks often begin in infancy or early childhood
and are precipitated by rest after exercise or by fasting. Attacks are usually shorter, more frequent, and less severe than
the hypokalemic form. Muscle spasms are common.
Is there any treatment?
Treatment of the periodic paralyses focuses on preventing further attacks and relieving acute symptoms. Avoiding carbohydrate-rich
meals and strenuous exercise, and taking acetazolamide daily may prevent hypokalemic attacks. Attacks can be managed by drinking
a potassium chloride oral solution. Eating carbohydrate-rich, low-potassium foods, and avoiding strenuous exercise and fasting,
can help prevent hyperkalemic attacks
What is the prognosis?
The prognosis for the familial periodic paralyses varies. Chronic attacks may result in progressive weakness that persists
between attacks. Some cases respond well to treatment, which can prevent or reverse progressive muscle weakness
What research is being done?
The NINDS conducts and supports research on neuromuscular disorders such as the familial periodic paralyses. These studies
are aimed at increasing knowledge about these disorders and finding ways to prevent, treat, and cure them.
Synonyms: Periodic Paralyses