Thyrotoxic periodic paralysis is a condition in which there are episodes of muscle weakness in people with high levels of thyroid hormone (hyperthyroidism, thyrotoxicosis).
Alternative NamesPeriodic paralysis - thyrotoxic
Causes, incidence, and risk factorsThyrotoxic periodic paralysis is a rare condition that occurs only in people with high thyroid hormone levels (thyrotoxicosis). It is seen most commonly in Asian men.
There is a similar disorder, hypokalemic periodic paralysis (familial periodic paralysis). This is an inherited condition and does not have high thyroid levels.
Risk factors include a family history of periodic paralysis and hyperthyroidism.
SymptomsThyrotoxic periodic paralysis involves attacks of muscle weakness or paralysis alternating with periods of normal muscle function. Attacks usually begin after symptoms of hyperthyroidism have developed.
The frequency of attacks varies from daily to yearly. Episodes of muscle weakness may last for a few hours or several days.
Symptoms include:
People are alert during attacks. Normal strength returns between attacks.
Symptoms of hyperthyroidism:
The health care provider may suspect thyrotoxic periodic paralysis based on:
Diagnosis involves ruling out disorders associated with low potassium.
The health care provider may attempt to trigger an attack by giving you insulin and glucose (which reduces potassium levels) or thyroid hormone.
During an attack, there may be the following signs:
Between attacks, examination is normal. Or, there may be signs of hyperthyroidism, such as an enlarged thyroid.
Hyperthyroidism is confirmed by abnormal results on the following tests:
Other test results:
A muscle biopsymay occasionally show abnormalities.
TreatmentThe best treatment is to quickly reduce thyroid hormone levels. Potassium should also be given during the attack, preferably by mouth. If weakness is severe, intravenous potassium may be needed. (Note: intravenous potassium should be given only if kidney function is normal and the patient is monitored in the hospital.)
Weakness that involves the muscles used for breathing or swallowing is an emergency. Patients must be taken to a hospital. Dangerous heart arrhythmias may also occur during attacks.
Your health care provider may recommend that you eat a diet low in carbohydrates and salt to prevent attacks. Medications called beta blockers may reduce the number and severity of attacks while hyperthyroidism is brought under control.
Acetazolamide is effective in preventing attacks in people with familial periodic paralysis. It is usually not effective with thyrotoxic periodic paralysis.
Expectations (prognosis)Chronic attacks will eventually lead to muscle weakness that persists even between attacks. Thyrotoxic periodic paralysis responds well to treatment. Treating hyperthyroidism will prevent attacks and may even reverse muscle weakness.
ComplicationsGo to the emergency room or call the local emergency number (such as 911) if you have periods of muscle weakness. This is especially important if you have a family history of periodic paralysis or thyroid disorders.
Emergency symptoms include:
Genetic counseling may be advised. Treating the thyroid disorder prevents attacks of weakness.
is very rare and occurs mostly in young adult males of Asian ancestry around the third decade.
Familiar (genetic) Periodic paralysis comprises a group of rare genetic diseases that cause symptoms such as muscle weakness, muscle stiffness, and complete paralysis. While there more than 30 different strains of periodic paralysis have been identified, the most common include: * Hypokalemic Periodic Paralysis- Caused by reductions in potassium levels, causing the patient to experience weakness and paralysis after eating certain foods or strenuous exercise. * Thyrotoxic Periodic Paralysis- Associated with an overactive thyroid gland. * Hyperkalemic Periodic Paralysis- Weakness, paralysis, and stiffness is experienced after fasting or exercise. * Paramyotonia Congenita- Causes muscle stiffness or weakness as a result of cold temperatures, activity, or low potassium. * Potassium Aggravated Myotonia- Causes muscle stiffness as a result of ingesting potassium. * Malignant Hyperthermia-Caused by a reaction to drugs used in general anaesthetics. While diagnosis of partial paralysis can be extremely difficult, research is offering some new developments. Incidents of partial paralysis can be avoided by staying away from certain hormones, foods, and medications.
Hyperkalemic PP is also called potassium-sensitive PP.
A person with periodic paralysis experiences sudden onset of weakness, which gradually subsides, only to return again later.
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Periodic paralysis (PP) is the name for several rare, inherited muscle disorders marked by temporary weakness, especially following rest, sleep, or exercise.
Periodic paralysis disorders are genetic disorders that affect muscle strength. There are two major forms, hypokalemic and hyperkalemic, each caused by defects in different genes.
With hypokalemic periodic paralysis an attack of weakness can be induced by administering glucose and insulin with exercise. These tests are potentially hazardous and require careful monitoring.
The level of potassium in the blood rises slightly or is normal.
The level of potassium in the blood falls in the early stages of a paralytic attack.
Hypokalemic periodic paralysis is characterized by low levels of potassium in the blood during attacks, leading to muscle weakness or paralysis. In contrast, hyperkalemic periodic paralysis is characterized by high levels of potassium during episodes, resulting in muscle stiffness or weakness. Both conditions are genetic and involve dysfunction in ion channels that regulate potassium levels in muscle cells.
Electrical tests of muscle and a muscle biopsy show characteristic changes.