| ¿µ¹® | esotropia | ÇÑ±Û | ³»»ç½Ã |
|---|---|---|---|
| ¼³¸í | »ç½Ã Áß¿¡ ¾È±¸ÀÇ ÆíÀ§ ¹æÇâÀÌ ¾ÈÂÊÀ¸·Î ÆíÀ§µÈ »ç½Ã. Áï, ½Ã¼±À» ¹°Ã¼ ÂÊÀ¸·Î µ¹·Á ¹°Ã¼°¡ °¡Àå ¼±¸íÇÏ°Ô º¸ÀÏ ¼ö ÀÖµµ·Ï ÇÏ´Â ±â´ÉÀÎ ÁÖ½Ã(fixation)¸ñÇ¥¿¡ ´ëÇÏ¿© ÇÑÂÊ ´«ÀÇ ½Ã¼±ÀÌ ¾ÈÂÊÀ¸·Î ¹þ¾î³ª ÀÖ´Â »ç½Ã¸¦ ¸»ÇÑ´Ù. »ýÈÄ 6°³¿ù À̳»¿¡ ³ªÅ¸³ª´Â À¯¾Æ ³»»ç½Ã´Â ¾È±¸¸¦ ¿òÁ÷ÀÌ´Â ±ÙÀ°°ú ±× ±ÙÀ°ÀÇ ÀδëºÎÀ§ÀÇ ÀÌ»ó¿¡ ÀÇÇÑ ÇØºÎÇÐÀû ³»»ç½Ã°¡ ¸¹°í Ä¡·á ÈÄÀÇ ¿¹Èİ¡ ³ª»Ú´Ù. |
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| ¿µ¹® | congenital syphilis | ÇÑ±Û | ¼±Ãµ¸Åµ¶ |
|---|---|---|---|
| ¼³¸í | ÀӺΰ¡ ¸Åµ¶¿¡ °¨¿°µÇ¾î ÀÖÀ¸¸é ÀӽŠÈı⿡ ¸Åµ¶±ÕÀÌ Å¹ÝÀ» ÅëÇØ Ç÷Ç༺À¸·Î žƿ¡ °¨¿°(¼öÁ÷°¨¿°)µÈ °ÍÀ» ¸»ÇÏ´Ù. ´ëºÎºÐÀº À¯»ê, »ç»êÀÌ µÇÁö¸¸ Ãâ»ýÇϸé Á¦2±â ÀÌÈÄÀÇ ¹ßÁøÀ» º¸ÀδÙ. ¹ßÇö½Ã±â¿¡ µû¶ó¼ ¨ç žƸŵ¶, ¨è À¯¾Æ¸Åµ¶, ¨é ¸¸¹ß¼º ¼±Ãµ¸Åµ¶À¸·Î ºÐ·ùµÈ´Ù. ¨ç¿¡¼´Â »À¿¬°ñ¿°, °£-Áö¶ó ºñ´ë¿Í ¸Åµ¶¼º õÆ÷â, ¨è¿¡¼´Â ÆÄ·Î°¡¼º¸¶ºñ¿Í ¸Åµ¶¼º ÄÚ¿°, ¨é¿¡¼´Â ÇãÄ£½¼ ¼¼Â¡ÈÄ(ÇãÄ£½¼ Ä¡¾Æ, ¼Ó±Í¼º ³Ã», ½ÇÁú¼º °¢¸·¿°)¿¡ µû¶ó Ư¡ÀÌ ÀÖ´Ù. ±âŸ ¼öµÎÁõ, Áö´É¹ßÀ° ºÒ·® µîÀ» ÀÚÁÖ º¼ ¼ö ÀÖ´Ù. ¸Åµ¶ Ç÷û¹ÝÀÀÀº ´ëºÎºÐÀÇ °æ¿ì ¾ç¼ºÀ¸·Î ³ª¿Â´Ù. ¸Å¿ì µå¹°°Ô °£¼¼Æ÷³»¿¡¼ ¸Åµ¶±ÕÀ» ¹«¼öÈ÷ º¼ ¼ö ÀÖ´Ù. °£¼¼Æ÷ ÁÖº¯ÀÇ ¼¶À¯È¿Í ÇÔ²² ºÒ±ÔÄ¢ÇÑ ÈäÅÍ(hepar lobatum)¸¦ ¸¸µé ¼ö ÀÖ´Ù. |
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| ¿µ¹® | congenital rubella syndrome | ÇÑ±Û | ¼±ÃµÇ³ÁøÁõÈıº |
|---|---|---|---|
| ¼³¸í | ÀӽűⰣ Áß¿¡ »ê¸ð°¡ dzÁø¿¡ °É¸®¸é ÀÌ Ç³Áø ¹ÙÀÌ·¯½º´Â ŹÝÀ» ÅëÇØ¼ žƿ¡°Ô Àü´ÞµÇ¾î¼ žÆÀÇ Ç³Áø°¨¿°À» ÀÏÀ¸Å²´Ù. ÀӽŠù 3°³¿ù µ¿¾È, ƯÈ÷ ÀӽŠù´Þ¿¡ žư¡ dzÁøÀÇ °¨¿°À» ¹ÞÀ¸¸é, ½Å»ý¾Æ¿¡¼ ¼±Ãµ±âÇü, Áï ´«¿¡¼ ÃÐÁ¡À» Á¤È®È÷ ¸ÂÃß¾îÁÖ´Â ·»ÁîÀÇ ¿ªÇÒÀ» ÇÏ´Â ¼öÁ¤Ã¼ÀÇ È¥Å¹(¹é³»Àå), ½ÉÀå±âÇü, ±Í¸Ó°Å¸® ¹× ½ÉÇÑ Áö´É¹Ú¾àÀ» µ¿¹ÝÇÏ´Â ¼ÒµÎÁõ µîÀÌ ¹ß»ýÇÏ´Â ¼ö°¡ ¸¹´Ù. |
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| ¿µ¹® | congenital heart disease | ÇÑ±Û | ¼±Ãµ½ÉÀ庴 |
|---|---|---|---|
| ¼³¸í | ¼±ÃµÀûÀ¸·Î ½ÉÀåÀÇ ±¸Á¶¿¡ ÀÌ»óÀÌ ÀÖ´Â º´. |
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| CDH | 1) Chronic Daily Headache = CTH = ... |
|---|---|
| CDH | ceramide dihexoside; congenital diaphragmatic hernia; congenital dislocation of hip; congenital dysp... |
| ET | educational therapy; effective temperature; ejection time; embryo transfer; endothelin; endotoxin; e... |
| RET | reticular; reticulocyte; retina; retention; retained; right esotropia |
| ST | esotropia; scala tympani; scaphotrapezoid; sclerotherapy; sedimentation time; semitendinosus; sensor... |
| CCHB | Complete congenital heart block |
|---|---|
| C.C.A.M. | Congenital Cystic Adenomatoid Malformation |
| CDH | Congenital Diaphragmatic Hernia |
| CDH | Congenital Dislocation of the Hip |
| CDG | Congenital Disorders of Glycosylation |
| A-esotropia | Convergent strabismus greater in upward than in downward gaze. (05 Mar 2000) |
|---|---|
| basic esotropia | That type of esotropia not influenced by correction of refractive error. Synonym: basic esotropia. (05 Mar 2000) |
| V-esotropia | Convergent strabismus greater in downward than in upward gaze. (05 Mar 2000) |
| refractive accommodative esotropia | That type of esotropia eliminated by correction of hypermetropic refractive error. (05 Mar 2000) |
| mixed esotropia | <ophthalmology> That type of esotropia in which both accommodative and nonaccommodative factors are present. (05 Mar 2000) |
| consecutive esotropia | Esotropia that follows surgical correction of exotropia. (05 Mar 2000) |
| cyclic esotropia | Periodic convergent strabismus often occurring every 48 hours. Synonym: alternate day strabismus. (05 Mar 2000) |
| X-esotropia | Decreasing convergence from the primary position in both upward and downward gaze. (05 Mar 2000) |
| nonaccommodative esotropia | That type of esotropia not influenced by correction of refractive error. Synonym: basic esotropia. (05 Mar 2000) |
| nonrefractive accommodative esotropia | That type of esotropia in which an abnormality of the accommodative-convergence mechanism is not eliminated by correction of refractive error. (05 Mar 2000) |
| esotropia | Cross-eyed. (27 Sep 1997) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
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