Familial Periodic Paralysis
NB : 3 types based upon plasma [K+]
- Hypokalaemic : < 3.0 mmol/L
- inherited - familial periodic paralysis
- acquired
- precipitated by large meals
- post-exercise
- glucose/insulin infusion
- catecholamines
- *common
- Normokalaemic : ≈ 3.0-5.5 mmol/L
- precipitated by alcohol, exercise and stress
- Hyperkalaemic : > 5.5 mmol/L
- precipitated by exercise (? release of K+ from muscle)
- K+ infusions
- hypothermia (decreased activity of Na+/K+ pump)
- usually localised to tongue and eyelids
Causes of Episodic Paralysis
- myasthenia gravis
- myasthenic syndrome
- thyrotoxicosis
- hyperaldosteronism
- antibiotics
- botulinism
- multiple sclerosis
- familial periodic paralysis
- TIA, RIND
- hysterical
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