| 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. |
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| 영문 | benign | 한글 | 양성 |
|---|---|---|---|
| 설명 | 치유가 잘 되는, 종양의 경우에서는 다른 조직으로 퍼지지 않고 그부분에서 머물러 있는 종양을 말한다. |
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| 영문 | benign tumor | 한글 | 양성종양 |
|---|---|---|---|
| 설명 | 발육속도가 완만하여 성장에 한계가 있고, 주위와의 경계가 명확하며, 다른 조직으로 퍼지지 않으며, 침윤이나 전이를 일으키지 아니하는 종양. 섬유종이나 지방종 따위가 전형적인 예이다. 양성종양은 종양이 존재한다고 해도 1차적으로 숙주의 생명을 위협하는 일은 없다. 양성종양의 발육형식은 주위의 조직간에 왕래하는 일이 없이 주위의 조직을 밀어내며 증식한다. 발육속도는 완만하며 전이하거나 절제 후 재발하는 일이 극히 드물다. 종양성분은 변이체이긴 하지만 성숙한 정상세포와 거의 다른 것이 없다. 전신에 대한 영향은 악성종양의 경우 어느 정도 발육했을 때 전신의 영양상태가 손상되어 카켁시아가 되지만 양성종양의 경우 이런 일은 거의 없다. 양성종양과 악성종양의 성상의 차이에 엄밀한 경계는 없고, 경계경변으로 보이는 종양도 있다. |
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| 영문 | Benign Prostatic Hyperplasia(BPH) | 한글 | 전립샘비대 |
|---|---|---|---|
| 설명 | 50세 이상의 남성에 빈발하는 병으로 전립샘의 요도 주위 영역에 큰결절을 형성하여, 이것이 커지면 요도를 압박하여 부분적 혹은 완전한 요도폐색을 일으키는 병이다. 증상은 요도폐색에 따른 소변의 감소와 방광자극증상으로 빈뇨, 잔뇨감, 소변을 참을 수 없는 증상 등이다. 치료는 경요도 전립샘 적출술로 전립선의 비대한 부분을 절제해야 한다. |
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| BPV | benign paroxysmal vertigo; benign positional vertigo; bioprosthetic valve; bovine papilloma virus |
|---|---|
| CRSM | cherry red spot myoclonus |
| DME | degenerative myoclonus epilepsy; dimethyl diester; dimethyl ether; diphasic meningoencephalitis; dir... |
| JME | juvenile myoclonus epilepsy |
| MERRF | myoclonus epilepsy with ragged red fibers [syndrome] |
| MERRF | Myoclonus epilepsy associated with ragged-red fibers |
|---|---|
| MERRF | Myoclonus epilepsy with ragged-red fibers |
| PME | Progressive Myoclonus Epilepsy |
| MERRF | myoclonus epilepsy and ragged red fiber |
| EIEE | Early infantile epileptic encephalopathy |
| 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) |
| aggressive infantile fibromatosis | A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize. (05 Mar 2000) |
| autism, infantile | A syndrome beginning in infancy and characterised by a lack of responsiveness to other people, gross impairment in verbal and nonverbal communication skills, and bizarre responses to the environment. (12 Dec 1998) |
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| spasms, infantile | Primary generalised epileptic seizures occurring in infants between birth and twelve months of age consisting of brief synchronous contractions of the neck, torso, and both arms. These seizures often occur in infants with underlying neurologic diseases. The prognosis for these infants is grave, with approximately ninety percent developing mental retardation in addition to their seizures. The eeg has a typical hypsarrhythmia pattern. The spasms and hypsarrhythmia have a tendency to disappear over the first three to five years of life, only to be replaced by other forms of generalised seizures. Infantile spasms sometimes respond to valproic acid or acth. (12 Dec 1998) |
| supravalvar aortic stenosis-infantile hypercalcaemia syndrome | <syndrome> Supravalvar aortic stenosis associated with elfin facies, mental retardation, and hypercalcaemia; usually sporadic; perhaps an irregular dominant trait. (05 Mar 2000) |
| diffuse infantile familial sclerosis | <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia Synonym: Krabbe leukodystrophy (12 Dec 1998) |
| infantile | Pertaining to an infant or to infancy. Origin: L. Infantilis (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|