| 영문 | epilepsy | 한글 | 간질 |
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| 설명 | 돌발적이고 일과적인 발작을 특징으로 하는 만성 중추신경계 질환의 총칭이며 공통적으로 운동, 지각, 자율신경계 혹은 정신 증상을 나타내고 거의 모든 경우에 비정상적인 뇌파 양상을 나타낸다. 뇌조직의 병터 또는 기능적인 장애로 인하여 발작적으로 신경기능장애를 일으켜 여러 가지 신경증상, 즉 돌발적인 의식상실, 경련, 정신 또는 감각장애를 일으키는 질환, 전간 또는 지랄병이라고도 한다. 전인구의 약 0.5%~1%에서 볼 수 있는 흔한 질병으로서, 종전엔 유전병이나 불치의 병으로 단정하여 치료를 기피하는 경향이 있었다. 그러나 간질의 원인과 치료면에서 근래에 많은 발전이 있어 현재는 약물치료와 뇌수술로써 간질 환자의 약 80%를 치유할 수 있다. 간질은 뇌의 이상이나, 이에 따른 특징적인 신체증상도 같이 나타난다. 다양한 형태가 있으며, 뇌파검사상 전반적인 뇌전체의 이상이 나타나면 전신발작(generalized seizure(=epilepsy))이라고 하며, 일부의 뇌에서 이상이 나타나면 부분발작(partial seizure)이라고 한다. 또한 전신발작에는 큰 팔다리의 운동과 의식소실, 자율신경이상 등을 호소하는 가장 심한 형태의 대발작(grand mal seizure)와, 잠깐의 의식소실만을 호소하는 소발작(petit mal seizure)가 있다. 그리고 부분발작에는 운동부위에만 이상이 나타나는 운동발작(motor seizure), 감각부위에만 이상이 나타나는 감각발작(sensory seizure), 그리고 관자엽의 이상뇌파소견을 나타내는 관자엽 발작(temporal lobe seizure) 등이 있다. 3세 소아에 일어나고, 단순히 의식소실(5~10초간)을 나타낸다. |
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| TLE | Temporal Lobe Epilepsy; 측두엽 간질 = Psychomotor Epilepsy; 정신 운동 간질 = Tem... |
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| MERRF Syndrome | Myoclonic Epilepsy & Ragged Red Fibers Syndrome |
| SME | severe myoclonic epilepsy |
| SMEI | severe myoclonic epilepsy of infancy |
| ASAB | Anti-Sperm Anti-Bodies |
| JME | Juvenile Myoclonic Epilepsy |
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| MERRF | Myoclonic Epilepsy and Ragged Red Fibers |
| MERRF | Myoclonic epilepsy with ragged-red fibers |
| PME | Progressive myoclonic epilepsy |
| SMEI | Severe myoclonic epilepsy in infancy |
| myoclonic astatic epilepsy | A petit mal variant characterised by atonic (drop attacks) and tonic or tonic-clonic attacks in neurologically disabled (hemiplegic, ataxic, etc.) children with mental retardation; characterised in EEG by 2/sec spike and wave discharges; usually progresses in spite of medication. (05 Mar 2000) |
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| epilepsy, myoclonic | A progressive encephalopathy characterised by myoclonic jerks (single or repetitive muscle contractions involving one body part or the entire body), mental retardation, and ataxia. The disease, an autosomal recessive form of epilepsy, occurs usually at puberty. The most significant pathological findings are lafora's inclusion bodies, which contain mucopolysaccharides. (12 Dec 1998) |
| epilepsy with myoclonic absences | A form of generalised epilepsy characterised by absence seizures, severe bilateral rhythmic clonic jerks often associated with tonic contraction, and an EEG 3 Hz spike and wave pattern. Age of onset is usually around seven years and males are more often affected. (05 Mar 2000) |
| juvenile myoclonic epilepsy | An epilepsy syndrome typically beginning in early adolescence, and characterised by early morning myoclonic jerks that may progress into a generalised tonic-clonic seizure. A genetic disorder: some families have had gene linkage to chromosome-6. The EEG is characterised by generalised polyspike and wave discharges at 4-6 Hz. (05 Mar 2000) |
| Lafora body | An intraneural intracytoplasmic inclusion body composed of acid mucopolysaccharides, seen in familial myoclonus epilepsy; a recessive trait. (05 Mar 2000) |
| Lafora body disease | A form of progressive myoclonus epilepsy beginning from age 6 to 19; characterised by generalised tonic-clonic seizures, resting and action myoclonus, ataxia, dementia, and classic EEG findings, including polyspike and wave discharges; basophilic cytoplasmic inclusion bodies present in portions of the brain, the liver, and skin, as well as the duct cells of the sweat glands. Death usually occurs within 10 years of onset; autosomal recessive inheritance. Synonym: Lafora's disease. (05 Mar 2000) |
| Lafora, Gonzalo Rodriguez | <person> Spanish neurologist, 1887-1971. See: Lafora body, Lafora body disease, Lafora's disease. (05 Mar 2000) |
| Lafora's disease | A form of progressive myoclonus epilepsy beginning from age 6 to 19; characterised by generalised tonic-clonic seizures, resting and action myoclonus, ataxia, dementia, and classic EEG findings, including polyspike and wave discharges; basophilic cytoplasmic inclusion bodies present in portions of the brain, the liver, and skin, as well as the duct cells of the sweat glands. Death usually occurs within 10 years of onset; autosomal recessive inheritance. Synonym: Lafora's disease. (05 Mar 2000) |
| myoclonic | Showing myoclonus. (05 Mar 2000) |
| myoclonic seizure | Seizure associated with single or repetitive myoclonic jerks. (05 Mar 2000) |
| anosognosic epilepsy | Epilepsy characterised by attacks of which the person is unaware. Synonym: anosognosic seizures. (05 Mar 2000) |
| automatic epilepsy | <neurology> Seizures with elaborate and multiple sensory, motor, and/or psychic components. A common feature is the clouding of consciousness and amnesia for the event. Some clinical manifestations may include more complex behaviours like burst of anger, emotional outbursts, fear or automatisms. The EEG often reveals spike discharges in the temporal lobe during sleep. (02 Jan 1998) |
| autonomic epilepsy | Episodes of autonomic dysfunction presumably due to diencephalic irritation. Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy. (05 Mar 2000) |
| benign childhood epilepsy with centrotemporal spikes | A specific epilepsy syndrome beginning in childhood and remitting in adolescence, characterised by nocturnal simple partial motor seizures or generalised tonic-clonic seizures. EEG shows centrotemporal spikes that are activated by sleep and an otherwise normal EEG background. (05 Mar 2000) |
| major epilepsy | tonic-clonic seizure |
| Lafora's bodies, myoclonic epilepsy (disease), sign |
see under body, epilepsy, and sign.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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