| deform | deformed, deformity |
|---|---|
| JRA | Juvenile Rheumatoid Arthritis; 연소기 류마토이드 관절염 = Juvenile Chronic Arthritis; 연소기 만성 관절... |
| JD | jejunal diverticulitis; juvenile delinquent; juvenile diabetes |
| CAP | camptodactyly-arthropathy-pericarditis [syndrome]; Canada Assistance Plan; capsule; captopril; catab... |
| HPA | Health Care Practice Act; Health Policy Agenda for the American People; health promotion advocates; ... |
| Dfd | Deformed |
|---|---|
| AR-JP | Autosomal recessive juvenile parkinsonism |
| GJP | Generalized Juvenile Periodontitis |
| IJ | infective juvenile |
| JA | Juvenile Arthritis |
| arthropathy | <rheumatology> Any disease that affects joints. Origin: Gr. Pathos = disease (11 Nov 1997) |
|---|---|
| arthropathy, neurogenic | Chronic progressive degeneration of the stress-bearing portion of a joint, with bizarre hypertrophic changes at the periphery. It is probably a complication of a variety of neurologic disorders, particularly tabes dorsalis, involving loss of sensation, which leads to relaxation of supporting structures and chronic instability of the joint. (12 Dec 1998) |
| static arthropathy | Secondary involvement of a joint following disease in a joint of the same extremity; e.g., knee or ankle involvement in hip disease. (05 Mar 2000) |
| neuropathic arthropathy | <radiology> M more than F, age more than 40 yrs, 6 D's, destruction, increased density, dislocation, debris, distension, disorganization, diabetic neuropathy, syphilis (tabes dorsalis), syrinx, meningomyelocele / spina bifida, nerve injury: spinal cord or peripheral nerves, congenital insensitivity to pain, leprosy, Charcot-Marie-Tooth syndrome (12 Dec 1998) |
| diabetic arthropathy | A neuropathic arthropathy occurring in diabetes. (05 Mar 2000) |
| tabetic arthropathy | A neuropathic arthropathy that occurs with tabes dorsalis (tabetic neurosyphilis). See: neuropathic joint. Synonym: Charcot's joint. (05 Mar 2000) |
| Jaccoud's arthropathy | A rare form of chronic arthritis, reported to occur after attacks of acute rheumatic fever, characterised by an unusual form of bone erosion of the metacarpal heads and by ulnar deviation of the fingers; it resembles rheumatoid arthritis, but with less overt inflammation, and rheumatoid factor is absent. Synonym: Jaccoud's arthropathy. (05 Mar 2000) |
| long-leg arthropathy | A degenerative joint disease that develops, after many years, in the knee of the longer leg of a person with unequal leg lengths. (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) |
| systemic-onset juvenile rheumatoid arthritis | <rheumatology> A form of joint disease, arthritis, that presents with systemic upset. Clinical signs: 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 itself may not be immediately apparent but once apparent, it may persist after the systemic symptoms have resolved. Synonym: Still's disease. (03 Jul 1999) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|