| ¿µ¹® | fit, paroxysmal | ÇÑ±Û | ¹ßÀÛ, ÀûÀÀ, ÀûÇÕ |
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| ECG | Electro-Cardio-Graphy(-Gram); ½ÉÀüµµ = EKG 1. Conducting System Structu... |
|---|---|
| AREPA | acetazolamide-responsive familial paroxysmal ataxia |
| FHH | Familial Hypocalciuric Hypercalcemia = Familial Benign Hypercalcemia |
| FAD | familial Alzheimer dementia; familial autonomic dysfunction; fetal activity-acceleration determinati... |
| FAP | familial adenomatous polyposis; familial amyloid polyneuropathy; fatty acid polyunsaturated; fatty a... |
| B.P.P.V. | Benign Paroxysmal Positional Vertigo |
|---|---|
| BPPV | Benign paroxysmal positioning vertigo |
| CPH | Chronic Paroxysmal Hemicrania |
| PAF | Paroxysmal Atrial Fibrillation |
| PDC | Paroxysmal Dystonic Choreoathetosis |
| familial recurrent polyserositis | familial paroxysmal polyserositis |
|---|---|
| familial paroxysmal rhabdomyolysis | acute recurrent rhabdomyolysis |
| recurrent polyserositis | Familial Mediterranean fever. (05 Mar 2000) |
| periodic polyserositis | familial paroxysmal polyserositis |
| polyserositis | Chronic inflammation with effusions in several serous cavities resulting in fibrous thickening of the serosa and constrictive pericarditis. Synonym: Bamberger's disease, Concato's disease, multiple serositis. Origin: poly-+ L. Serum, serum, + G. -itis, inflammation Familial paroxysmal polyserositis, transient recurring attacks of abdominal pain, fever, pleurisy, arthritis, and rash; the condition is asymptomatic between attacks; autosomal recessive inheritance. There is an autosomal dominant recessive in which amyloidosis in common. Synonym: benign paroxysmal peritonitis, familial Mediterranean fever, familial recurrent polyserositis, Mediterranean fever, periodic peritonitis, periodic polyserositis. (05 Mar 2000) |
| benign paroxysmal peritonitis | familial paroxysmal polyserositis |
| benign paroxysmal postural vertigo | A recurrent, brief form of postural vertigo occurring in clusters; believed to result from displaced remnants of utricular otoconia. Synonym: cupulolithiasis. (05 Mar 2000) |
| paroxysmal | <cardiology, neurology> Recurring in paroxysms, spasms or seizures. (18 Nov 1997) |
| paroxysmal atrial tachycardia | Bouts of rapid, regular heart beating originating in the atrium (upper chamber of the heart). Due to abnormalities in the av node relay station that lead to rapid firing of electrical impulses from the atrium which bypass the av node under certain conditions. These conditions include alcohol excess, stress, caffeine, overactive thyroid or excessive thyroid hormone intake, and certain drugs. Pat is an example of an arrhythmia where the abnormality is in the electrical system of the heart, while the heart muscle and valves may be normal. (12 Dec 1998) |
| paroxysmal cerebral dysrhythmia | A diffusely abnormal electroencephalogram often seen with epilepsy. (05 Mar 2000) |
| paroxysmal cold haemoglobinuria | <haematology> A rare blood disorder caused by antibodies which destroy red blood cells upon exposure to the cold. The antibodies are formed against a specific blood group and are triggered by the cold. The cause is unknown but the disease has been associated with syphilis and some viral infections. Serum haemoglobin and urine haemoglobin are increased during the attacks. The disease is chronic and treatment is difficult. Some cases resolve spontaneously without treatment. Origin: Gr. Ouron = urine (27 Sep 1997) |
| paroxysmal nocturnal dyspnea | Acute dyspnea appearing suddenly at night, usually waking the patient after an hour or two of sleep; caused by pulmonary congestion with or without oedema that results from left-sided heart failure following immobilization of fluid from dependent areas after lying down. (05 Mar 2000) |
| paroxysmal nocturnal dyspnoea | <cardiology> Wakening in the middle of the night with shortness of breath. A symptom of left ventricular failure. (15 Nov 1997) |
| paroxysmal nocturnal haemoglobinuria | An infrequent disorder with insidious onset (usually in the third or fourth decade) and chronic course, characterised by episodes of haemolytic anaemia, haemoglobinuria (chiefly at night), pallor, icterus or bronzing of the skin, a moderate degree of splenomegaly, and sometimes hepatomegaly; red blood cells are usually macrocytic and vary considerably in size, but there is no evidence of spherocytosis, erythrophagocytosis, or abnormal leukocytes. The disorder is a result of an abnormality of the red cell membrane which makes the red cell unusually sensitive to lysis by complement. Synonym: Marchiafava-Micheli anaemia, Marchiafava-Micheli syndrome. (05 Mar 2000) |
| paroxysmal sleep | <neurology> A disorder of sleep associated with excessive daytime sleepiness, involuntary daytime sleep episodes, disturbed nocturnal sleep and cataplexy. Narcolepsy affects over 100,000 people in the United States and appears to have a genetic basis. Symptoms usually begin in the patients twenties. Treatment often includes the use of amphetamines and-or tricyclic antidepressants. (27 Sep 1997) |
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