Periodic paralysis (hyperkalaemic)
Hyperkalaemic periodic paralysis is an autosomal dominantly inherited disease where there are attacks of paralysis lasting 30 or 40 minutes.
During the attacks the potassium rises, but some patients show weakness at serum potassium concentrations not greater than 4mM.
Attacks may be aborted by IV calcium gluconate.
Related pages
Create an account to add page annotations
Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.