| ¿µ¹® | septal defects of heart | ÇÑ±Û | ½ÉÀåÀÇ Áß°Ý °á¼Õ |
|---|---|---|---|
| ¼³¸í | ¼±ÃµÀûÀ¸·Î ½ÉÀå ³»ÀÇ ½É¹æ»çÀÌÁß°Ý(interatrial septum)À̳ª ½É½Ç»çÀÌÁß°Ý(interventricular septum)ÀÌ °á¼ÕµÇ¾î Ç÷·ù°¡ Á¤»óÀûÀ¸·Î È帣Áö ¾Ê´Â °æ¿ì. Á¤»óÀûÀÎ °æ¿ì Ç÷·ù´Â Á¤¸Æ¿¡¼ ¿ì½É¹æÀ¸·Î ¸ð¿© ¿ì½É½ÇÀ» °ÅÄ£µÚ Æó·Î °¡¼ »ê¼Ò¸¦ °ø±Þ¹Þ°í ´Ù½Ã ¿Þ½É¹æ, ¿Þ½É½ÇÀ» Â÷·Ê·Î °ÅÃÄ ´ëµ¿¸ÆÀ¸·Î °£´Ù. ÇÏÁö¸¸, ÀÌ °æ¿ì´Â Ç÷·ù°¡ ¾Ð·ÂÀÌ ³ôÀº ¿Þ½É¹æÀ̳ª ¿Þ½É½Ç¿¡¼ ¾Ð·ÂÀÌ ³·Àº ¿ì½É¹æÀ̳ª ¿ì½É½Ç·Î È帣°Ô µÈ´Ù. µû¶ó¼ µ¿¸ÆÇÇ¿Í Á¤¸ÆÇǰ¡ ¼¯ÀÌ°Ô µÇ°í, ȯÀڴ ȣÈí°ï¶õ, ¼ºÀå¹ßÀ°Àå¾Ö, ½ÉÀâÀ½ µîÀÌ ³ªÅ¸³ª°í, ½ÉÇÑ °æ¿ì û»öÁõÀ¸·Î ¹ßÀüÇϱ⵵ ÇÑ´Ù. Ä¡·á´Â ¼ö¼úÀûÀ¸·Î ÀÌ °á¼ÕºÎÀ§¸¦ ¸·¾Æ ÁÖ¾î¾ß ÇÑ´Ù. |
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| ¿µ¹® | complement | ÇÑ±Û | º¸Ã¼ |
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| ¼³¸í | Ç×ü¿Í ¹ÝÀÀÇÏ¿© Ç×ü¿Í °áÇÕµÈ ¼¼Æ÷ÀÇ ÆÄ±«¸¦ ÀÏÀ¸Å°´Â ´Ü¹éÁúÀ» ¸»ÇÑ´Ù. Ç×ü°¡ Ç×ü¿Í °áÇÕÇÑ ¼¼Æ÷¸¦ ÆÄ±«ÇÏ´Â ¹æ¹ý¿¡´Â ¿©·¯ °¡Áö°¡ Àִµ¥ ±× ÁßÀÇ Çϳª·Î Ç×ü¿Í °áÇÕÇÑ ¼¼Æ÷ÀÇ Ç¥¸éÀ» ºÎºÐÀûÀ¸·Î ¼Õ»ó½ÃÄÑ ±× ¼¼Æ÷¸¦ ÆÄ±«ÇÏ´Â ¿ªÇÒÀ» ÇÏ´Â °ÍÀÌ ÀÌ º¸Ã¼ÀÌ´Ù. º¸Ã¼´Â 20°¡ÁöÀÇ ´Ü¹éÁú·Î ±¸¼ºµÇ¾î Àִµ¥ ¾àÀÚ·Î C·Î Ç¥½ÃÇÏ¸ç °¢ Á¾·ù¸¦ ³ªÅ¸³¾ °æ¿ì¿¡´Â C¿·¿¡ ¼ýÀÚ¸¦ ½á¼ Ç¥½ÃÇÑ´Ù. |
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| ¿µ¹® | complement fixation reaction | ÇÑ±Û | º¸Ã¼°áÇÕ ¹ÝÀÀ, µµ¿òü°áÇÕ¹ÝÀÀ |
|---|---|---|---|
| ¼³¸í | Ç×ü¿ÍÀÇ ¹ÝÀÀ¿¡ ÀÖ¾î¼ º¸Ã¼¿Í °áÇÕÇÏ´Â Ç×ü¸¦ °Ë»çÇÏ´Â ¹æ¹ýÀ¸·Î, ÀÌ ¹ÝÀÀÀº ÃÖÃÊ¿¡ ±âÁöÇ׿ø, ÇǰËÇ÷û ¹× º¸Ã¼¸¦ È¥ÇÕÇÑ´Ù. Á¦2´Ü°è¿¡¼´Â ÀûÇ÷±¸¿Í À̰Ϳ¡ ´ëÀÀÇÏ´Â ¿ëÇ÷¼ÒÀÇ È¥ÇÕ¾×À» °¡ÇÑ´Ù. º» ¹ÝÀÀÈÄ ¿ëÇ÷ÀÌ ÀϾÁö ¾ÊÀ¸¸é º»Ã¼´Â Ç׿øÇ×ü°áÇÕ¹°¿¡ °áÇÕÇÑ °ÍÀÌ µÇ¾î ¾ç¼ºÀÌ µÇÁö¸¸, ¿ëÇ÷ÀÌ ÀÏ¾î³ °æ¿ì º¸Ã¼´Â °áÇÕÇÏÁö ¾Ê¾Æ ¼ÒºñµÇÁö ¾Ê±â ¶§¹®¿¡ À½¼ºÀÌ µÈ´Ù. º» ¹ÝÀÀÀº ±âÁöÇ÷ûÀ» ½á¼ Ç׿ø°ËÃâ¿¡ ÀÀ¿ëÇÒ ¼ö ÀÖÀ¸¸ç, ¸¶ÀÌÄÚÇö󽺸¶, ¸®ÄÉÃ, Ŭ¶ó¹Ìµð¾Æ, ¹ÙÀÌ·¯½º, ¸Åµ¶ µîÀÇ Áø´Ü¿¡ ¾²ÀδÙ. |
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| ¿µ¹® | hepatic portal system | ÇÑ±Û | °£¹®¸Æ°è |
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| ¼³¸í | À§, ÀÛÀºÃ¢ÀÚÀ̳ª ūâÀÚ¿¡¼ ¿µ¾çºÐÀ» Èí¼öÇϱâ À§ÇÑ ¸ð¼¼Ç÷°üÁ¶Á÷Àº ¸ðµÎ °£À¸·Î ¿¬°áµÈ´Ù. Áï ¼Òȱ⿡ Èí¼öÇÑ ¿µ¾çºÐÀÌ °¡µæÇÑ ÇÇ´Â ¸ðµÎ °£À¸·Î ¿¬°áµÇ´Âµ¥ À̰ÍÀ» ¹®¸Æ°è¶ó°í ÇÑ´Ù. |
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| ¿µ¹® | system | ÇÑ±Û | °è, °èÅë |
|---|---|---|---|
| ¼³¸í | ÀÎü¸¦ ±¸¼ºÇÏ´Â °è´Â ´ÙÀ½°ú °°ÀÌ ±¸ºÐµÈ´Ù. 1) ½ÉÀåÇ÷°ü°èÅë(cardiovascular system) 2) È£Èí±â°è(respiratory system) 3) ¼Òȱâ°è(digeshive system) 4) ºñ´¢±â°è(urinary system) 5) »ý½Ä±â°è(genital system) 6) Ç÷¾×°è(hematologic system) 7) ³»ºÐºñ°è(endocrine system) 8) ½Å°æ°è(nervous system) 9) °ñ°Ý°è(skeletal system) 10) ±ÙÀ°°è(muscular system) 11) ÇǺΰè(integumentary system). |
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| PHAVER | pterygia-heart defects-autosomal recessive inheritance-vertebral defects-ear anomalies-radial defect... |
|---|---|
| ISIS | image selected in vivo spectroscopy; imaging science and information system; information system-imag... |
| CRL | cell repository line; Certified Record Librarian; complement receptor location; complement receptor ... |
| MDS | Master of Dental Surgery; maternal deprivation syndrome; medical data screening; medical data system... |
| MPS | meconium plug syndrome; medial premotor system; Member of the Pharmaceutical Society; microbial prof... |
| AVSD | Atrio ventricular septal defects |
|---|---|
| BDMP | Birth Defects Monitoring Program |
| LRD | Limb reduction defects |
| MACDP | Metropolitan Atlanta Congenital Defects Program |
| MLS | Microphthalmia with linear skin defects |
| complement system | A group of more than 20 serum proteins, some of which can be serially activated and participate in a cascade resulting in cell lysis. (05 Mar 2000) |
|---|---|
| gastric filling defects | <radiology> Malignant tumours, carcinoma, lymphoma, leiomyosarcoma, metastases, benign, leiomyoma, lipoma, neurofibroma, polyp, hyperplastic, adenomatous, hamartomatous, others, bezoar, Nissen fundoplication, ectopic pancreas (12 Dec 1998) |
| midline closure defects | <radiology> Anencephaly, encephalocele, 70% occipital, 20% parietal or frontal, 10% basal, agenesis of corpus callosum associated with increased alpha-fetoprotein. (12 Dec 1998) |
| colour vision defects | Mild to severe impairment in the ability to discriminate or differentiate hues. This disorder may be acquired as a result of diseases of the cones or x chromosome-linked where there is an abnormality but not a complete absence of one of the cone pigments. (12 Dec 1998) |
| heart defects, congenital | Imperfections or malformations of the heart, existing at birth. (12 Dec 1998) |
| heart septal defects | Defects in the cardiac septa, resulting in abnormal communications between the opposite chambers of the heart. (12 Dec 1998) |
| heart septal defects, atrial | Defects in the septum between the atria of the heart, due to failure of fusion between either the septum secundum or the septum primum and the endocardial cushions. (12 Dec 1998) |
| heart septal defects, ventricular | Congenital defects in the septum between the cardiac ventricles, most often due to failure of the bulbar septum to completely close the interventricular foramen. (12 Dec 1998) |
| endocardial cushion defects | A spectrum of septal defects associated with persistence of the embryonic atrioventricular canal due to incomplete growth and fusion of the endocardial cushion. (12 Dec 1998) |
| furcation defects | Conditions in which a bifurcation or trifurcation of the molar tooth root becomes denuded as a result of periodontal disease. It may be followed by tooth mobility, temperature sensitivity, pain, and alveolar bone resorption. (12 Dec 1998) |
| male chromosome complement | The large majority of males have a 46, xy chromosome complement (46 chromosomes including an x and a y chromosome). A minority of males have other chromosome constitutions such as 47,xxy (47 chromosomes including two x chromosomes and a y chromosome) and 47,xyy (47 chromosomes including an x and two y chromosomes). (12 Dec 1998) |
| genetic complement | <biology, genetics> The set of chromosomes contained within any one particular cell. (07 May 1998) |
| receptors, complement | Molecules on the surface of some B-lymphocytes and macrophages, that recognise and combine with the c3b, c3d, c1q, and c4b components of complement. (12 Dec 1998) |
| receptors, complement 3b | Molecular sites on or in some B-lymphocytes and macrophages that recognise and combine with complement 3b. The primary structure of these receptors reveal that they contain transmembrane and cytoplasmic domains, with their extracellular portion composed entirely of thirty short consensus repeats each having 60 to 70 amino acids. (12 Dec 1998) |
| receptors, complement 3d | Molecular sites on or in B-lymphocytes, follicular dendritic cells, lymphoid cells, and epithelial cells that recognise and combine with complement 3d. Human cr2 serves as a receptor for both c3dg and the gp350/220 glycoprotein of herpes virus 4, human, and binds the monoclonal antibody okb7, which blocks binding of both ligands to the receptor. (12 Dec 1998) |
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