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Hypokalemic periodic paralysis
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| Hypokalemic periodic paralysis |
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Definition:
Hypokalemic periodic paralysis is an inherited disorder that causes occasional episodes of muscle weakness. Alternative Names:
Periodic paralysis - hypokalemic
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Causes, incidence, and risk factors:
Hypokalemic periodic paralysis is a condition of intermittent episodes of muscle weakness and sometimes severe paralysis. It is one of a group of genetic disorders that includes hyperkalemic periodic paralysis and thyrotoxic periodic paralysis. This disorder is distinguished from other forms of periodic paralysis in that people with this disorder have normal thyroid function and very low blood levels of potassium during episodes of weakness.
Hypokalemic periodic paralysis is a congenital (present from birth) condition. It can be inherited but occasionally occurs as a result of a non-inherited genetic mutation that affects just the sperm or the egg cell. In most cases, it is inherited as an autosomal dominant disorder (only one parent must transmit the gene for the baby to be affected).
The disorder involves attacks of muscle weakness or paralysis alternating with periods of normal muscle function. Attacks usually begin in adolescence, but they can occur before age 10. Attacks of intermittent weakness that do not begin until adulthood are rare and are usually caused by other disorders. The frequency of attacks varies from daily to yearly. Episodes of muscle weakness usually last between a few hours and one day. Other forms of periodic paralysis may last longer.
During an attack of muscle weakness, there is a low level of potassium in the bloodstream. Serum potassium levels are normal between attacks. There is no decrease in total body potassium, however. Potassium flows from the bloodstream into muscle cells during attacks.
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