| ¿µ¹® | septal defects of heart | ÇÑ±Û | ½ÉÀåÀÇ Áß°Ý °á¼Õ |
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| 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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| PHAVER | pterygia-heart defects-autosomal recessive inheritance-vertebral defects-ear anomalies-radial defect... |
|---|---|
| VATER Associations | Vertebral defects Anal atresia Tracheo-Esophageal fistula ... |
| AEC | ankyloblepharon, ectodermal defects, and cleft lip [syndrome]; at earliest convenience; Atomic Energ... |
| ARBD | alcohol-related birth defects |
| CHILD | congenital hemidysplasia with ichthyosiform erythroderma and limb defects [syndrome] |
| 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 |
| 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) |
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