- symptoms begin early in life (before age 25) and follow
rest or sleep rather than exertion
- alertness is completely preserved during attacks &
power is normal between attacks
hypokalaemic form
- predominantly inherited but can also arise sporadically
- involvement of bulbar or respiratory muscles is rare but can occur
- hypokalaemia during attacks is generally mild but symptoms
clinical periodic -the term periodic paralysis describes a group
respond rapidly to potassium supplementation features paralysis general of rare primary inherited disorders that are mostly
autosomal dominant and cause periodic weakness
- acetazolamide provides effective prophylaxis
[created
hyperkalaemic form
- milder and almost always inherited by Paul - in general the underlying abnormality is
- virtually never requires intensive care Young pathogenesis a defect in a skeletal muscle ion channel
- responds to carbohydrate administration
- thiazides or acetazolamide provide effective prophylaxis 29/11/07]
- usually successful in both preventing attacks and
preventing chronic weakness which may develop treatment
after many years of attacks in untreated patients