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Thyrotoxic periodic paralysis

Periodic paralysis - thyrotoxic; Hyperthyroidism - periodic paralysis

Thyrotoxic periodic paralysis (TPP) is a condition with episodes of severe muscle weakness. It occurs in people who have high levels of thyroid hormone in their blood. Examples of this include hyperthyroidism and thyrotoxicosis.


Thyroid gland

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This rare condition occurs only in people with high (usually very high) thyroid hormone levels (thyrotoxicosis). Men of Asian or Hispanic descent are affected more often. Most people who develop high thyroid hormone levels are not at risk of periodic paralysis.

Hypokalemic, or familial, periodic paralysis is a similar disorder. It is an inherited condition and not related to high thyroid levels, but has the same symptoms.

Risk factors include a family history of periodic paralysis and hyperthyroidism.


Symptoms involve attacks of muscle weakness or paralysis. Between attacks, normal muscle function returns. Attacks often begin after symptoms of hyperthyroidism have developed. Hyperthyroid symptoms may be subtle.

The attacks may occur daily to yearly. Episodes of muscle weakness or paralysis may:

Other rare symptoms may include any of the following:

During attacks, you will be alert and can answer questions. Normal strength returns between attacks. With repeated attacks, you may develop muscle weakness.

Symptoms of hyperthyroidism include:

Exams and Tests

Your health care provider may suspect TPP based on:

Diagnosis involves ruling out disorders caused by low blood potassium.

Your provider may try to trigger an attack by giving you insulin and sugar. The sugar is glucose, which reduces your potassium level. Or you may be given thyroid hormone.

The following signs may be seen during the attack:

Between attacks, the examination is normal. Or, there may be signs of hyperthyroidism. These include an enlarged thyroid, changes in the eyes, tremors, or hair and nail changes.

The following tests are used to diagnose hyperthyroidism:

Other test results:

A muscle biopsy may sometimes be taken.


Potassium should be given during the attack, most often by mouth. If weakness is severe, you may need to get potassium through a vein (IV).

Note: You should only get IV potassium if your kidney function is normal and you are monitored in the hospital.

Weakness that involves the muscles used for breathing or swallowing is an emergency. People must be taken to a hospital. Serious irregularity of the heartbeat also occurs during attacks.

Your provider may recommend a diet low in carbohydrates and salt to prevent attacks. You may be given beta-blocker medicines to reduce the number and severity of attacks while your hyperthyroidism is brought under control.

Acetazolamide is effective at preventing attacks in people with familial periodic paralysis. It is usually not effective for TPP.

Outlook (Prognosis)

If an attack isn't treated and the breathing muscles are affected, death can occur.

Chronic attacks over time can lead to muscle weakness. This weakness can continue even between attacks if the thyrotoxicosis is not treated.

TPP responds well to treatment. Treating hyperthyroidism will prevent attacks. It may even reverse muscle weakness.

Possible Complications

Untreated TPP can lead to:

When to Contact a Medical Professional

Call 911 or the local emergency number or go to the emergency room 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.

Related Information

Hypokalemic periodic paralysis
Muscle function loss
Muscle cramps
Potassium test
Breathing difficulty


Hollenberg A, Wiersinga WM. Hyperthyroid disorders. In: Melmed S, Auchus RJ, Goldfine AB, Koenig RJ, Rosen CJ, eds. Williams Textbook of Endocrinology. 14th ed. Philadelphia, PA: Elsevier; 2020:chap 12.

Kang MK, Kerchner GA, Ptacek LJ. Channelopathies: Episodic and electrical disorders of the nervous system. In: Jankovic J, Mazziotta JC, Pomeroy SL, Newman NJ, eds. Bradley and Daroff's Neurology in Clinical Practice. 8th ed. Philadelphia, PA: Elsevier; 2022:chap 98.

Selcen D. Muscle diseases. In: Goldman L, Cooney KA, eds. Goldman-Cecil Medicine. 27th ed. Philadelphia, PA: Elsevier; 2024:chap 389.

Weetman AP, Kahaly GJ. Graves disease. In: Robertson RP, ed. DeGroot's Endocrinology. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 71.


Review Date: 2/28/2024  

Reviewed By: Sandeep K. Dhaliwal, MD, board-certified in Diabetes, Endocrinology, and Metabolism, Springfield, VA. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

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