| JAS | Jenkins Activity Survey; juvenile ankylosing spondylitis |
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| AS | 1) Aortic Stenosis ; LV 와 Aorta 사이의 압력차 ... |
| HLA | Human Leukocyte Antigen; 인백혈구 항원 ? HLA B27 Ag (+)로 나오는 경우... |
| AS | acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis... |
| ASP | abnormal spinal posture; acute symmetric polyarthritis; African swine pox; aged substrate plasma; al... |
| AS | Ankylosing Spondylitis |
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| BASDAI | Bath Ankylosing Spondylitis Disease Activity Index |
| BASFI | Bath Ankylosing Spondylitis Functional Index |
| AS | Ankylosing Spondylarthritis |
| AR-JP | Autosomal recessive juvenile parkinsonism |
| ankylosing spondylitis | <rheumatology> A polyarthritis involving the spine, which is characterised by progressive, painful stiffening of the joints and ligaments. It almost exclusively affects young men. Interestingly the disease seems to be associated with HLA B27, those with this histocompatability antigen are 300 times more likely to get the disease, 90% of sufferers have HLA B27 (18 Nov 1997) |
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| spondylitis, ankylosing | The form of rheumatoid arthritis affecting the spine. It occurs predominantly in young males and produces pain and stiffness as a result of inflammation of the sacroiliac, intervertebral, and costovertebral joints. Aetiology is unknown. (12 Dec 1998) |
| ankylosing hyperostosis | A form of degenerative arthritis characteristically associated with flowing calcification along the sides of the vertebrae of the spine and commonly with inflammation (tendinitis) and calcification of the tendons at their attachments points to bone. Because areas of the spine and tendons can become inflamed, antiinflammatory medications (NSAIDs), such ibuprofen, can be helpful in both relieving pain and inflammation. Also called Forestier's disease. (12 Dec 1998) |
| arthritis, spondylitis | A form of arthritis causing chronic inflammation of the spine. (12 Dec 1998) |
| rheumatoid spondylitis | <rheumatology> A polyarthritis involving the spine, which is characterised by progressive, painful stiffening of the joints and ligaments. It almost exclusively affects young men. Interestingly the disease seems to be associated with HLA B27, those with this histocompatability antigen are 300 times more likely to get the disease, 90% of sufferers have HLA B27 (18 Nov 1997) |
| spondylitis | <pathology> Inflammation of the vertebrae. (18 Nov 1997) |
| spondylitis deformans | Arthritis and osteitis deformans involving the spinal column; marked by nodular deposits at the edges of the intervertebral disks with ossification of the ligaments and bony ankylosis of the intervertebral articulations, it results in a rounded kyphosis with rigidity. Synonym: Bechterew's disease, poker back, Strumpell's disease. (05 Mar 2000) |
| tuberculous spondylitis | Tuberculous infection of the spine associated with a sharp angulation of the spine at the point of disease. Synonym: Pott's disease, spondylarthrocace, spondylocace, trachelocyrtosis, trachelokyphosis. (05 Mar 2000) |
| Kummell's spondylitis | Late posttraumatic collapse of a vertebral body. (05 Mar 2000) |
| arthritis, juvenile rheumatoid | Rheumatoid arthritis of children occurring in three major subtypes defined by the symptoms present during the first six months following onset: systemic-onset (still's disease, juvenile-onset) polyarticular-onset, and pauciarticular-onset. Adult-onset cases of still's disease (still's disease, adult-onset) are also known. Only one subtype of juvenile rheumatoid arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. (12 Dec 1998) |
| benign juvenile melanoma | A benign, slightly pigmented or red superficial small skin tumour composed of spindle-shaped, epithelioid, and multinucleated cells that may appear atypical; most common in children, but also appearing in adults. Synonym: benign juvenile melanoma, epithelioid cell nevus, spindle cell nevus. (05 Mar 2000) |
| rheumatoid arthritis, systemic-onset juvenile | Also known as systemic-onset juvenile chronic arthritis. Still's disease presents with systemic (bodywide) illness including high intermittent fever, a salmon-coloured skin rash, swollen lymph glands, enlargement of the liver and spleen, and inflammation of the lungs (pleuritis) and around the heart (pericarditis). The arthritis may not be immediately apparent but it does appear and may persist after the systemic symptoms are gone. (12 Dec 1998) |
| periodontitis, juvenile | Localised periodontitis in teenagers and young adults. The onset is during the circumpubertal period but the diagnosis can be made beyond puberty. Lesions are confined predominantly to the first permanent molars or incisors and the distribution of lesions is usually symmetrical. The gingiva may appear normal. The lesions are highly active immediately following puberty but later destruction may slow or cease spontaneously. The disease is four times more prevalent in females than males and more prevalent in african americans than in other races or ethnic groups. (12 Dec 1998) |
| xanthogranuloma, juvenile | Benign disorder of infants and children characterised by multiple nodules with lipid-laden, non-langerhans-cell histiocytes. (12 Dec 1998) |
| systemic-onset juvenile chronic arthritis | See: Systemic-onset juvenile rheumatoid arthritis (still's disease). (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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