| 영문 | myoclonus | 한글 | 간대성근경련(증) |
|---|---|---|---|
| 설명 | 근육의 일부, 근육 전체, 또는 일군의 근육의 갑작스러운 수축으로서 신체의 일부영역에 제한되거나, 혹은 여러 부위에서 동시성 또는 비동시성으로 나타난다. |
||
| ADEE | age-dependent epileptic encephalopathy |
|---|---|
| CROME | congenital cataracts-epileptic fits-mental retardation [syndrome] |
| E-ADD | epileptic attentional deficit disorder |
| EIEE | early infantile epileptic encephalopathy |
| epil | epilepsy, epileptic |
| EIEE | Early infantile epileptic encephalopathy |
|---|---|
| ES | Epileptic seizures |
| MERRF | Myoclonus epilepsy associated with ragged-red fibers |
| MERRF | Myoclonus epilepsy with ragged-red fibers |
| NES | Non-Epileptic Seizure |
| acquired epileptic aphasia | <syndrome> Acquired epileptic aphasia. The typical history is that of a child whose development is normal for several years and then, either suddenly or in a fluctuating manner, loses comprehension of speech and the ability to use speech to communicate. The seizures are of no specific type, and are mostly mild and infrequent partial or atypical absences. (12 Dec 1998) |
|---|---|
| epileptic | 1. One affected with epilepsy. 2. A medicine for the cure of epilepsy. Source: Websters Dictionary (01 Mar 1998) |
| epileptic dementia | Dementia occurring in an individual afflicted with epilepsy, and thought to be a result of prolonged seizures, the epileptogenic brain lesion, or antiepileptic drugs. Hebephrenic dementia, dementia with hebephrenic symptoms. (05 Mar 2000) |
| epileptic seizure | A seizure that is caused by epilepsy. (05 Mar 2000) |
| Baltic myoclonus disease | One of the familial light sensitive myoclonic epilepsies. Unlike Lafora body polymyoclonus, where inclusion bodies are seen in the brain cells, the prognosis is often favourable. Probably an autosomal recessive disorder. (05 Mar 2000) |
| palatal myoclonus | Rhythmic contractions of the soft palate, the facial muscles, and the diaphragm, related to lesions of the olivocerebellar pathways. See: palatal nystagmus. (05 Mar 2000) |
| cherry-red spot myoclonus syndrome | <syndrome> A neuronal storage disorder in children characterised by a cherry red spot at the macula, progressive myoclonus, and easily controlled seizures; the result of sialidase deficiency. Type 1 is characterised by normal body habitus, cherry red macula, myoclonus, and normal beta-galactosidase levels; type 2 by short stature, bony abnormalities, and deficient beta-galactosidase. Synonym: sialidosis. (05 Mar 2000) |
| myoclonus | Twitching or spasm of a muscle or a group of muscles. (27 Sep 1997) |
| myoclonus epilepsy | A clinically diverse group of epilepsy syndromes, some benign, some progressive. Many are hereditary with mendelian and nonmendelian mitochondrial inheritance. All are characterised by the occurrence of myoclonus, which may be limited or predominate in the condition. Specific syndromes include cherry red spot myoclonus syndrome, ceroid lipofuscinosis, myoclonic epilepsy with ragged red fibres, and Baltic myoclonus. Synonym: localization related epilepsy. (05 Mar 2000) |
| myoclonus multiplex | An ill-defined disorder marked by rapid and widespread muscle contractions. Synonym: paramyoclonus multiplex, polyclonia, polymyoclonus. (05 Mar 2000) |
| stimulus sensitive myoclonus | Myoclonus induced by a variety of stimuli, e.g., talking, calculation, loud noises, tapping, etc. (05 Mar 2000) |
| nocturnal myoclonus | Frequently repeated muscular jerks occurring at the moment of dropping off to sleep. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|