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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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Periodic paralysis

Periodic paralysis
  Hypokalemic periodic paralysis Thyrotoxic periodic paralysis Hyperkalemic periodic paralysis Andersen syndrome
Age at onset First or second decade >20 years First decade First or second decade
Attack frequency Infrequent (a few times a year) Infrequent Frequent (up to several a day) Monthly
Attack duration Hours to days Hours to days Minutes to hours Days
Precipitants

Exercise

Carbohydrate load

Stress

Others*

Exercise

Carbohydrate load

Stress

Others*

Exercise

Fasting

Stress

K-rich food
Rest after exercise
Potassium level during attack Low Low Normal or elevated Low, normal, or elevated
Associated features Later-onset myopathy

Symptoms of thyrotoxicosis

Low TSH with high T4 or high T3

Myotonia on examination and/or EMG

Later-onset myopathy

Dysmorphic features

Ventricular arrhythmias

Long QT interval
Etiology Autosomal dominant inherited defect in calcium or sodium ion channel on muscle membrane

Thyrotoxicosis

Possible inherited predisposition
Autosomal dominant inherited defect of sodium ion channel on muscle membrane Autosomal dominant inherited defect of inward rectifying potassium channel
Penetrance Nonpenetrance common, especially in females   High Nonpenetrance and incomplete penetrance common
Epidemiology Clinical expression in males more frequent than females Highest incidence in individuals from East Asia (eg, China, Japan) and in males more than females Sexes equally affected Marked intrafamilial phenotypic variation
Preventive treatment

Carbonic anhydrase inhibitors

K-sparing diuretics

Euthyroid state

Propranolol

Carbonic anhydrase inhibitors

Thiazide diuretics

Inhaled beta-agonists as needed
Carbonic anhydrase inhibitors

K: potassium; TSH: thyroid-stimulating hormone; T4: thyroid hormone (thyroxine); T3: thyroid hormone (triiodothyronine); EMG: electromyography.

* Refer to UpToDate topics on periodic paralysis.
Graphic 65215 Version 3.0

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