| PAIN | pyoderma gangrenosum, aphthous stomatitis, inflammatory eye disease, erythema nodosum [disorders ass... |
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| PG | paregoric; parotid gland; pentagastrin; pepsinogen; peptidoglycan; Pharmacopoeia Germanica; phosphat... |
| JRA | Juvenile Rheumatoid Arthritis; 연소기 류마토이드 관절염 = Juvenile Chronic Arthritis; 연소기 만성 관절... |
| JD | jejunal diverticulitis; juvenile delinquent; juvenile diabetes |
| HSM Syndrome | juvenile-familial Endocrinopathy Hypoparathyroidism Addison's Disease Menillansis |
| PG | Pyoderma Gangrenosum |
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| AR-JP | Autosomal recessive juvenile parkinsonism |
| GJP | Generalized Juvenile Periodontitis |
| IJ | infective juvenile |
| JA | Juvenile Arthritis |
| chancriform pyoderma | A persistent, necrotizing, ulcerated, single pyogenic lesion, usually on the face or genitalia. (05 Mar 2000) |
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| primary pyoderma | A pyoderma, such as impetigo, in which pus formation is an essential part of the disease. (05 Mar 2000) |
| secondary pyoderma | A pyoderma in which an existing skin lesion (eczema, herpes, seborrheic dermatitis, etc.) becomes secondarily infected. (05 Mar 2000) |
| pyoderma | <dermatology> Any purulent skin disease. Synonym: pyodermia. (18 Nov 1997) |
| pyoderma gangrenosum | An ulcerating condition of skin resulting in heaped borders with a typical appearance. Pyoderma gangrenosum appears to be mediated by the immune system, but the exact cause is unknown. The lesion(s) usually begin as a soft nodule on the skin which proceeds to ulcerate. The ulcer enlarges and the skin at the edge is purple-red. Ulcers can become quite large. This condition is associated with several other diseases, some of which are ulcerative colitis, crohn's disease, rheumatoid arthritis, leukaemia, and cryoglobulinaemia. Pyoderma gangrenosum is usually responsive to corticosteroids. (12 Dec 1998) |
| pyoderma vegetans | A benign fungating granulomatous mass caused by chronic pyogenic infection. Synonym: pyoderma vegetans. (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) |
| juvenile | Pertaining to youth or childhood, young or immature. (18 Nov 1997) |
| juvenile absence epilepsy | A generalised epilepsy syndrome with onset around puberty, characterised by absence seizures and generalised tonic-clonic seizures. EEG often shows a greater than 3 Hz generalised spike wave pattern. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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