| 영문 | muscular dystrophy | 한글 | 근육퇴행위축 |
|---|---|---|---|
| 설명 | 근섬유의 파괴로 인한 점진적인 근위축과 허약을 특징으로 하는 일련의 선천적인 질환군을 통털어 말한다. 대표적인 경우가 뒤쉔(Duchenne)형으로 성염색체 열성유전을 하며, 대개 4 세이내에 발병해 청년기를 넘기는 경우가 드물다. 특징적 소견으로 장딴지근(gastronemius)의 거짓비대(pseudohypertrophy)(실제적으로는 근위축이 일어나지만, 근섬유 대신에 지방세포가 들어차 도리어 마치 근육이 증가한 것처럼 보이는 현상) 소견을 볼 수 있다. |
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| INAD | infantile neuroaxonal dystrophy |
|---|---|
| LIAFI | late infantile amaurotic familial idiocy |
| LA | lactic acid; large amount; laser angioplasty; late abortion; late antigen; latex agglutination; left... |
| LAR | laryngology; late asthmatic response; late reaction; left arm recumbent; leukocyte antigen-related |
| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| INAD | Infantile neuroaxonal dystrophy |
|---|---|
| NAD | Neuroaxonal dystrophy |
| LINCL | Late infantile neuronal ceroid lipofuscinosis |
| EIEE | Early infantile epileptic encephalopathy |
| IHPS | Infantile Hypertrophic Pyloric Stenosis |
acute angle
| infantile neuroaxonal dystrophy | <neurology, paediatrics> A rare, familial disorder of early childhood manifested as progressive psychomotor deterioration, increased reflexes, Babinski sign, hypotonia and progressive blindness. Pathologically, eosinophilic spheroids of swollen axoplasm are found in various central nervous system nuclei. (05 Mar 2000) |
|---|---|
| neuroaxonal dystrophy | A rare disorder that begins in the second year of life and is relentlessly progressive; clinically characterised initially by walking difficulties, weakness, and areflexia, later followed by corticospinal and pseudobulbar findings, blindness, loss of pain appreciation, and mental deterioration; pathologically, eosinophilic spheroids of swollen axoplasm are found in various central nuclei; autosomal recessive inheritance. (05 Mar 2000) |
| neuroaxonal dystrophies | Encephalopathies characterised by swelling in distal portions of axons (speroids) often with axonal degeneration. Neuroaxonal dystrophy is seen in various genetic diseases, vitamin deficiencies, and aging. Infantile neuroaxonal dystrophy (seitelberger's disease) is an autosomal recessive trait characterised by arrested psychomotor development at 6 months to 2 years followed by ataxia, brainstem signs, optic atrophy, and quadriparesis. Hallervorden-spatz syndrome, which usually first appears at 7 to 12 years of age, may be genetically related to the infantile syndrome. (12 Dec 1998) |
| receptors, very late antigen | Members of the integrin family appearing late after T-cell activation. They are a family of proteins initially identified at the surface of stimulated T-cells, but now identified on a variety of cell types. At least six vla antigens have been identified as heterodimeric adhesion receptors consisting of a single common beta-subunit and different alpha-subunits. (12 Dec 1998) |
| late apical systolic murmur | A murmur previously considered benign, or even extracardiac, with a possible relationship to pericardial disease; it often represents mitral insufficiency, often localised and of moderate severity but with propensity for developing bacterial endocarditis, and is frequently associated with systolic click and mitral prolapse (Barlow syndrome; a balloon or billowing mitral valve leaflet) often producing a click, murmur, or both, as it prolapses during systole into the left atrium. (05 Mar 2000) |
| late benign syphilis | Late syphilis, manifested by serologic evidence of infection, but without any clinical manifestations. (05 Mar 2000) |
| late cyanosis | cyanose tardive |
| late deceleration | Any transient foetal bradycardia, the nadir of which occurs after the peak of the uterine contraction. (05 Mar 2000) |
| late diastole | That part of diastole immediately preceding systole. Synonym: late diastole. (05 Mar 2000) |
| late diastolic murmur | A murmur heard at the end of ventricular diastole (during atrial systole if in sinus rhythm), usually due to obstruction at one of the atrioventricular orifices. Synonym: atriosystolic murmur, late diastolic murmur. (05 Mar 2000) |
| late effect | Side effects of chemotherapy and/or radiotherapy which only become apparent with long-term monitoring of the patient over a period of years. These are of particular concern in patients below the age of puberty. (18 Nov 1997) |
| late gene | <genetics, molecular biology> Gene expressed relatively late after infection of a host cell by a virus, usually structural proteins for the viral coat. (18 Nov 1997) |
| late latent syphilis | Usually infectious in pregnant women only, who may pass the infection on to the foetus. (05 Mar 2000) |
| late luteal phase dysphoric disorder | <syndrome> A combination of emotional, physical, psychological, and mood disturbances that occur after ovulation and normally end with the onset of the menstrual flow. (12 Dec 1998) |
| late-phase response | Recurrence of symptoms after an appreciable interval following challenge with an antigen; preceded by an initial early-phase response. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|