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hypokalemic periodic paralysis
(redirected from Primary Hypokalemic Periodic Paralysis)

   Also found in: Wikipedia 0.01 sec.
paralysis /pa·ral·y·sis/ (pah-ral´ĭ-sis) pl. paral´yses   loss or impairment of motor function in a part due to lesion of the neural or muscular mechanism; also, by analogy, impairment of sensory function (sensory p.) .
paralysis a´gitans  Parkinson's disease.
ascending paralysis  spinal paralysis that progresses cephalad.
bulbar paralysis  progressive bulbar palsy.
compression paralysis  that caused by pressure on a nerve.
conjugate paralysis  loss of ability to perform some parallel ocular movements.
crossed paralysis , cruciate paralysis that affecting one side of the face and the other side of the body.
decubitus paralysis  that due to pressure on a nerve from lying for a long time in one position.
divers' paralysis  decompression sickness.
Duchenne's paralysis 
Erb-Duchenne paralysis  paralysis of the upper roots of the brachial plexus, caused by birth injury.
facial paralysis  weakening or paralysis of the facial nerve, as in Bell's palsy.
familial periodic paralysis  a rare inherited disorder with recurring attacks of rapidly progressive flaccid paralysis associated with serum potassium levels that are decreased (type I or hypokalemic type), increased (type II or hyperkalemic type), or normal (type III or normokalemic type).
hyperkalemic periodic paralysis  see familial periodic p.
hypokalemic periodic paralysis  see familial periodic p.
immune paralysis , immunologic paralysis older name for immunologic tolerance.
juvenile paralysis agitans (of Hunt)  increased muscle tonus with the characteristic attitude and facies of paralysis agitans, occurring in early life and due to progressive degeneration of the globus pallidus.
Klumpke's paralysis , Klumpke-Dejerine paralysis lower brachial plexus paralysis caused by birth injury, particularly during a breech delivery.
Landry's paralysis  acute idiopathic polyneuritis.
mixed paralysis  combined motor and sensory paralysis.
motor paralysis  paralysis of voluntary muscles.
musculospiral paralysis  paralysis of the extensor muscles of the wrist and fingers.
normokalemic periodic paralysis  see familial periodic p.
periodic paralysis 
1. any of various diseases characterized by episodic flaccid paralysis or muscular weakness.
postepileptic paralysis  Todd's p.
progressive bulbar paralysis  see under palsy.
pseudobulbar paralysis  spastic weakness of the muscles innervated by the cranial nerves, i.e., the facial muscles, pharynx, and tongue, due to bilateral lesions of the corticospinal tract, often accompanied by uncontrolled weeping or laughing.
pseudohypertrophic muscular paralysis  see under dystrophy.
sensory paralysis  loss of sensation due to a morbid process.
thyrotoxic periodic paralysis  recurrent episodes of generalized or local paralysis accompanied by hypokalemia, occurring in association with Graves' disease, especially after exercise or a high carbohydrate or high sodium meal.
Todd's paralysis  transient hemiplegia or monoplegia after an epileptic seizure.
vasomotor paralysis  cessation of vasomotor control.

hy·po·ka·le·mic periodic paralysis (hp-k-lmk)
n.
An inherited form of periodic paralysis characterized by attacks in which the serum potassium level is low and respiratory paralysis may occur. Onset usually occurs between the ages of 7 and 21 years.

hypokalemic periodic paralysis
Etymology: Gk, hypo, under; L, kalium, potassium; Gk, peri, near, hodos, way, paralyein, to be palsied
a state of recurring attacks of muscular weakness associated with low blood levels of potassium.

hypokalemic periodic paralysis
Familial periodic paralysis, see there


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Engel AG, Lambert EH: Calcium activation of electrically inexcitable muscle fibres in primary hypokalemic periodic paralysis.
 
 
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