| 영문 | osteoporosis | 한글 | 뼈다공증 |
|---|---|---|---|
| 설명 | 뼈조직의 감소로 뼈에 구멍이 난 상태를 말한다. 주로 칼슘염의 감소로 기인하여 뼈가 얇아지고 약해진다. 따라서 뼈의 골절이 잘 발생하게 된다. 이런 현상은 나이많은 폐경기의 여자에서 잘 발생한다. 이 이유는 월경이 일어나지 않는 폐경상태에서는 여성호르몬(에스트로겐)의 분비가 감소되는데, 에스트로겐의 감소가 뼈의 뼈파괴세포(osteoclast)의 활동을 증가시켜 뼈의 파괴를 촉진하고 뼈의 칼슘침착을 감소시킨다. 이에 대한 치료는 여성호르몬의 투여로써 가능하다. |
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| ABCDES | abnormal alignment, bones-periarticular osteoporosis, cartilage-joint space loss, deformities, margi... |
|---|---|
| JRA | Juvenile Rheumatoid Arthritis; 연소기 류마토이드 관절염 = Juvenile Chronic Arthritis; 연소기 만성 관절... |
| JD | jejunal diverticulitis; juvenile delinquent; juvenile diabetes |
| NOF | National Osteopathic Foundation; National Osteoporosis Foundation |
| OP | occipitoparietal; occipitoposterior; occiput posterior; octapeptide; olfactory peduncle; opening pre... |
| EVOS | European Vertebral Osteoporosis Study |
|---|---|
| OP | Osteoporosis |
| TOH | osteoporosis of the hip |
| AR-JP | Autosomal recessive juvenile parkinsonism |
| GJP | Generalized Juvenile Periodontitis |
| posttraumatic osteoporosis | Atrophy of bones, commonly of the carpal or tarsal bones, following a slight injury such as a sprain. See: causalgia, reflex sympathetic dystrophy. Synonym: acute reflex bone atrophy, posttraumatic osteoporosis, Sudeck's syndrome. Origin: L. English sweat (05 Mar 2000) |
|---|---|
| osteoporosis | <pathology> A reduction in the amount of bone mass, leading to fractures after minimal trauma. Origin: Gr. Poros = passage (18 Nov 1997) |
| osteoporosis, postmenopausal | Metabolic disorder associated with fractures of the femoral neck, vertebrae, and distal forearm. It occurs commonly in women within 15-20 years after menopause, and is caused by factors associated with menopause including oestrogen deficiency. (12 Dec 1998) |
| 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) |
| juvenile angiofibroma | <oncology, tumour> A benign tumour of the posterior nasopharynx that is most common in adolescent boys. Symptoms repeated epistaxis, nasal congestion, nasal discharge and hearing loss. A skull X-ray or a CT scan of the head can confirm the presence of an angiofibroma. Treatment may include the surgical removal of the lesion if it is enlarging or blocking the airway. (27 Sep 1997) |
| juvenile arrhythmia | <cardiology, physiology> An increase in heart rate during inspiration. A normal physiologic response, more pronounced in children. (27 Sep 1997) |
| juvenile carcinoma | <tumour> Carcinoma of the breast with pale-staining cells showing prominent secretory activity, as seen in pregnancy and lactation, but found mostly in children. Synonym: juvenile carcinoma. (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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