| 영문 | fibrous dysplasia | 한글 | 섬유형성이상 |
|---|---|---|---|
| 설명 | 국소 발육장애로 뼈의 모든 성분이 나타나나 성숙한 구조로 분화하지는 못하는 병이다. 임상으로 하나의 뼈 혹은 여러개의 뼈를 동시에 침범할 수 있다. 여러뼈 유형은 갈색색소 침착과 내분비 장애를 동반하며 조숙한 성적 발육을 동반한다. 육안소견으로 경계가 뚜렷한 병터로 조직소견으로는 섬유모세포의 증식과 곡선상의 뼈잔기둥으로 구성되어 있는데 뼈잔기둥은 뼈모세포로 덮여있지 않은 무층뼈(woven bone)이다. |
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| CSD | carotid sinus denervation; cat scratch disease; combined system disease; conditionally streptomycin ... |
|---|---|
| ASD | aldosterone secretion defect; Alzheimer senile dementia; antisiphon device; arthritis syphilitica de... |
| IASD | interatrial septal defect; inter-auricular septal defect |
| SD | Sandhoff disease; senile dementia; septal defect; serologically defined; serologically detectable; s... |
| MFH | Malignant Fibrous Histocytoma |
| FD | Fibrous dysplasia |
|---|---|
| MFH | malignant fibrous histocytoma |
| SFT | Solitary Fibrous Tumor |
| FS | fibrous sheath |
| ASD | Atrial septal defect |
cortical evoked potential (피질 유발 전위
| fibrous cortical defect | A common 1 to 3 cm defect in the cortex of a bone, most commonly the lower femoral shaft of a child, filled with fibrous tissue. Nonosteogenic or nonossifying fibroma by convention refers to lesions greater than 3 cm in diameter. See: nonossifying fibroma. Synonym: nonosteogenic fibroma. (05 Mar 2000) |
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| metaphysial fibrous cortical defect | A small (less than 2 to 3 cm in diameter) fibrous cortical d. (05 Mar 2000) |
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| acquired platelet function defect | <haematology> Platelet function can be affected by a number of different disease processes including polycythaemia vera, leukaemia, myelofibrosis, renal failure, multiple myeloma and some medications (for example penicillins, salicylates, phenothiazines). Disturbed blood clotting can be manifested by: easy bruising, bleeding gums, nosebleeds, abnormal vaginal bleeding, rectal bleeding, skin rash, vomiting blood, coughing up blood or blood in the urine. A measure of bleeding time and coagulation profile will be part of the evaluation. (29 Dec 1997) |
| aortic septal defect | A small congenital opening between the aorta and pulmonary artery about 1 cm above the semilunar valves, e.g., aorticopulmonary window. Synonym: aorticopulmonary window. (05 Mar 2000) |
| aortopulmonary septal defect | A congenital anomaly in which there is abnormal communication between the ascending aorta and pulmonary artery just above the semilunar valves. (12 Dec 1998) |
| atrial septal defect | <cardiology> An inherited condition where there is nonclosure of the foramen ovale at birth, resulting in congenital heart disease. Usually asymptomatic until the third or fourth decades of life. Symptoms include exertional shortness of breath, fatigue and palpitations. Acronym: ASD (12 Jan 1998) |
| atrial ventricular canal defect | A defect caused by deficient or absent septal tissue immediately above and below the normal level of the atrioventricular valves, including the region normally occupied by the A-V septum in hearts with two ventricles. The A-V valves are abnormal to a varying degree. (05 Mar 2000) |
| birth defect | Defect present at birth; sometimes referred to as congenital defect. (05 Mar 2000) |
| ventricular septal defect | <cardiology, embryology> A congenital heart defect where an abnormal opening exists in the ventricular septum. Blood flows from the higher pressure left ventricle (through the defect) into the right ventricle. (12 Jan 1998) |
| Gerbode defect | <cardiology, embryology> A defect in the interventricular portion of the membranous septum, associated with a communication between the right ventricle and the right atrium through an abnormality in the tricuspid valve. (05 Mar 2000) |
| mass defect | <chemistry, radiobiology> Of a nucleus, the difference between the sum of the masses of the constituent nucleons and the mass of the nucleus. (16 Dec 1997) |
| partial endocardial cushion defect | <radiology> Incomplete endocardial cushion defect components: ostium primum atrial septal defect, cleft in anterior mitral valve findings: right AV valve is usually normal, with or without mitral insufficiency, communication between LA_RA or LV-RA, occasionally LV-RV Cf: complete endocardial cushion defect (12 Dec 1998) |
| relative afferent pupillary defect | An asymmetry of the pupillomotor input between the two eyes; tested by alternating the light from one eye to the other and comparing the direct light reactions. (05 Mar 2000) |
| complete endocardial cushion defect | <radiology> Arteriovenous canal components: low atrial septal defect (ostium primum), high VSD, cleft anterior leaflet of mitral valve, cleft septal leaflet of tricuspid valve, one AV valve common to RV and LV with 5-6 leaflets findings: 4-chamber enlargement (R greater than L), mitral insufficiency, associated with congestive heart failure and Eisenmenger syndrome, gooseneck deformity on angiogram (elongation and narrowing of the LV outflow tract during diastole) see also: endocardial cushion defect, partial endocardial cushion defect (12 Dec 1998) |
| congenital defect | A birth defect. (12 Dec 1998) |
| congenital ectodermal defect | Incomplete development of the epidermis and skin appendages; the skin is smooth and hairless, the facies abnormal, and the teeth and nails may be affected; sweating may be deficient. Synonym: congenital ectodermal dysplasia. (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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