| GPI | general paralysis of the insane; glucose phosphate isomerase; glycoprotein I; glycosylphosphatidylin... |
|---|---|
| HLP | hepatic lipoperoxidation; hind leg paralysis; holoprosencephaly; hyperkeratosis lenticularis perstan... |
| HOKPP | hypokalemic periodic paralysis |
| HYPP | hyperkalemic periodic paralysis |
| LROP | lower radicular obstetrical paralysis |
| HypoPP | Hypokalaemic periodic paralysis |
|---|---|
| TPP | Thyrotoxic periodic paralysis |
| Brown-Sequard's paralysis | <neurology, syndrome> A type of spinal cord lesion that is characterised by hemiparaplegia and hyperesthesia, but with loss of motor function on the same side as the lesion and hemianaesthesia on the opposite side. (27 Sep 1997) |
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| bulbar paralysis | Progressive weakness and atrophy of the muscles of the tongue, lips, palate, pharynx, and larynx, usually occurring in later life; most often caused by motor neuron disease. Synonym: bulbar palsy, bulbar paralysis, Duchenne's disease, Erb disease, glossolabiolaryngeal paralysis, glossolabiopharyngeal paralysis. (05 Mar 2000) |
| vasomotor paralysis | A mild degree of vasoparalysis. Synonym: angioparesis, vasomotor paralysis. Origin: vaso-+ G. Paresis, weakness (05 Mar 2000) |
| generalised paralysis | Paralysis of both whole sides of the body; survival is usually of short duration. Synonym: generalised paralysis. (05 Mar 2000) |
| paralysis | <neurology> 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 paralysis). In addition to the types named below, paralysis is further distinguished as traumatic, syphilitic, toxic, etc., according to its cause or as obturator, ulnar, etc., according to the nerve part or muscle specially affected. Origin: Gr. Lyein = to loosen (18 Nov 1997) |
| paralysis agitans | An obsolete term for parkinsonism. (05 Mar 2000) |
| paralysis, bulbar | A paralysis resulting from changes in the motor centres of the medulla oblongata. It is chronic, usually fatal, and most commonly occurring in persons over 50 years old. (12 Dec 1998) |
| paralysis, familial periodic | An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis). (12 Dec 1998) |
| paralysis, obstetric | Paralysis of an infant resulting from injury received at birth. (12 Dec 1998) |
| ginger paralysis | Neuropathy produced by drinking synthetic Jamaican ginger (or "jake" in the vernacular) containing triorthocresylphosphate. Synonym: ginger paralysis. (05 Mar 2000) |
| parturient paralysis | A slight elevation of temperature following childbirth, said to be due to the establishment of the secretion of milk, but probably the same as absorption fever, an afebrile metabolic disease, occurring shortly after parturition in dairy cattle, characterised by hypocalcaemia and manifested by loss of consciousness and general paralysis. Synonym: parturient paralysis, parturient paresis. (05 Mar 2000) |
| global paralysis | Paralysis of both whole sides of the body; survival is usually of short duration. Synonym: generalised paralysis. (05 Mar 2000) |
| glossolabiolaryngeal paralysis | Progressive weakness and atrophy of the muscles of the tongue, lips, palate, pharynx, and larynx, usually occurring in later life; most often caused by motor neuron disease. Synonym: bulbar palsy, bulbar paralysis, Duchenne's disease, Erb disease, glossolabiolaryngeal paralysis, glossolabiopharyngeal paralysis. (05 Mar 2000) |
| glossopalatolabial paralysis | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles. Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis. (05 Mar 2000) |
| glossopharyngeolabial paralysis | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles. Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis. (05 Mar 2000) |