| 영문 | fit, paroxysmal | 한글 | 발작, 적응, 적합 |
|---|---|---|---|
| 설명 | 부적절하거나 불수의적인 운동성 또는 정신적 활동성을 특징으로 하는 발작상태. 병증세가 갑자기 나타났다가 비교적 짧은 시간에 사라지는 일. 간질이나 또는 어떤 종류의 마비 증세 등에서 볼 수 있다. 원인은 여러가지이겠지만, 대개의 경우 환자 자신의 의식이 분명하지 못하므로 주위사람들의 응급조치가 필요하다. 원칙적으로는 그대로 안정하도록 하여 쉬게 해주고, 옷을 헐겁게 풀어주며, 경우에 따라서는 혀를 깨물지 않도록 수건을 물리는 등의 조치를 취해야 한다. |
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| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = 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... |
| PDC | Paroxysmal Dystonic Choreoathetosis |
|---|---|
| PKC | Paroxysmal Kinesigenic Choreoathetosis |
| B.P.P.V. | Benign Paroxysmal Positional Vertigo |
| BPPV | Benign paroxysmal positioning vertigo |
| CPH | Chronic Paroxysmal Hemicrania |
| familial paroxysmal rhabdomyolysis | acute recurrent rhabdomyolysis |
|---|---|
| choreoathetosis | A condition characterised by aimless muscle movements and involuntary motions. (27 Sep 1997) |
| congenital choreoathetosis | A type of cerebral palsy manifested predominantly as bilateral involuntary movements, beginning at about the age of 3 years, and preceded by generalised hypotonia and delayed motor development. Due to various causes, including kernicterus and birth hypoxia. Synonym: congenital choreoathetosis, double congenital athetosis, Vogt syndrome. (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) |
| paroxysmal tachycardia | Recurrent attacks of tachycardia, with abrupt onset and often also abrupt termination, originating from an ectopic focus which may be atrial, A-V junctional, or ventricular. (05 Mar 2000) |
| haemoglobinuria, paroxysmal | Disorder characterised by intravascular haemolysis and haemoglobinuria. Some cases occur on exposure to cold and are due to the presence of an autohemolysin in the serum. Other cases are more marked during or immediately after sleep and are considered to be due to an acquired intracorpuscular defect. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|