| ¿µ¹® | cerebral infarction | ÇÑ±Û | ³ú°æ»öÁõ |
|---|---|---|---|
| ¼³¸í | ±Þ°ÝÇÑ Ç÷¾× °ø±ÞÀÇ Â÷´ÜÀ¸·Î ÀÎÇØ¼ Á¶Á÷ÀÌ Á×´Â °ÍÀ» ¸»ÇÑ´Ù. ³ú°æ»öÁõÀº ³úÀÇ Á¶Á÷ÀÌ Ç÷·ùÀÇ ±Þ°ÝÇÑ Â÷´Ü¿¡ ÀÇÇØ¼ Á×Àº °ÍÀ» ¸»ÇÑ´Ù. Ç÷·ù°¡ ¿ÏÀüÈ÷ Â÷´ÜµÇ¸é ±¹¼Ò¿¡ Ç÷¾×ÀÌ ¾ø¾îÁö¹Ç·Î ±× Á¶Á÷¿¡ °æ»öÀÌ »ý±â°Ô µÈ´Ù. °æ»öÀÌ »ý±ä ºÎÀ§´Â Ç÷¾×ÀÇ °ø±ÞÀÌ ¾øÀ¸¹Ç·Î ¿øÄ¢ÀûÀ¸·Î´Â Á¤»óÀûÀ¸·Î Ç÷·ù°¡ °ø±ÞµÇ´Â ºÎÀ§º¸´Ù â¹éÇϰí Èñ°Ô º¸ÀδÙ. ÀÌ·± ºÎºÐÀ» ¹é»ö°æ»ö(white infarct) ¶Ç´Â ºóÇ÷°æ»ö(anemic infarct)¶ó ÇÑ´Ù. ÇÏÁö¸¸ ÀÌ ºÎÀ§¿¡ ÀÌÂ÷ÀûÀ¸·Î ÀûÇ÷±¸°¡ ºüÁ® µé¾î°¡¸é ±× ºÎÀ§´Â Çǰ¡ °íÀÌ°Ô µÇ°í Àû»öÀ» ¶ì°Ô µÈ´Ù. ÀÌ·± ºÎºÐÀ» Àû»ö°æ»ö(red infarct) ¶Ç´Â ÃâÇ÷°æ»ö(hemorrhagic infarct)À̶ó°í ÇÑ´Ù. ³úÀÇ °æ»öÁõ¿¡´Â ÀÌ µÎ °¡Áö ¸ðµÎ ¹ß»ý°¡´ÉÇÏ´Ù. |
||
| ¿µ¹® | cerebral aneurysm | ÇÑ±Û | ³úµ¿¸Æ·ù, ³úµ¿¸ÆÀÚ·ç |
|---|---|---|---|
| ¼³¸í | ³úÀÇ µ¿¸Æ¿¡ »ý±ä µ¿¸ÆÀÚ·ç. ÀÓ»óÀûÀ¸·Î Áß¿ä½ÃµÇ´Â ÀÌÀ¯´Â À̰ÍÀÌ Àß ÅÍÁ® ³úÃâÇ÷ÀÇ Áß¿äÇÑ ¿øÀÎÀÌ µÇ±â ¶§¹®ÀÌ´Ù. ´ëºÎºÐÀÇ µ¿¸ÆÀÚ·ç°¡ ÃâÇ÷À» ÀÏÀ¸Å°Áö¸¸ ÃâÇ÷À» ÀÏÀ¸Å°Áö ¾Ê´Â °æ¿ì¿¡´Â ÁÖÀ§ÀÇ ³ú Á¶Á÷ÀÇ ¾Ð¹Ú¿¡ ÀÇÇØ¼ µÎÅëÀ̳ª ¹ßÀÛ µîÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù. |
||
| ¿µ¹® | cerebral palsy | ÇÑ±Û | ³ú¼º¸¶ºñ |
|---|---|---|---|
| ¼³¸í | Ãâ»ýÀü, Ãâ»ý½Ã ȤÀº Ãâ»ýÈÄÀÇ ³úÀÇ ¼±Ãµ±âÇü, ¼Õ»ó ȤÀº ÁßÃ߽Űæ°èÀÇ º´¿¡ ÀÇÇØ¼ ¿µ±¸ÀûÀ̸ç, ºñÁøÇ༺ÀÎ ¿îµ¿½Å°æ ¹× Á¤½ÅÀå¾Ö¸¦ ÀÏÀ¸Å°´Â °æ¿ì¸¦ ¶æÇÑ´Ù. ¿øÀÎÀº ¿©·¯ °¡Áö°¡ ÀÖÀ» ¼ö ÀÖÀ¸³ª Á¶»êÀ¸·Î ÀÎÇÑ ³úÀÇ »ê¼Ò°ø±ÞÀÇ ºÎÁ·, ¶Ç´Â ³»êÀ¸·Î ÀÎÇÑ È£ÈíÀå¾Ö µîÀÌ ÈçÇÑ ¿øÀÎÀÌ´Ù. Áõ»óÀº ´ë°³ ºñÁøÇ༺ÀÇ ³ú º´º¯À¸·Î ÀÎÇÑ ¿îµ¿Àå¾Ö°¡ ´ëÇ¥ÀûÀÎ Áõ»óÀÌ¸ç ±×¿Ü¿¡ û·Â, ½Ã·ÂÀÇ Àå¾Ö, Áö´ÉºÎÀü, ¾ð¾îÀå¾Ö, °æ·Ã ¹× Á¤½ÅÀå¾Ö µîÀÌ µ¿¹ÝµÉ ¼ö ÀÖ´Ù. |
||
| ¿µ¹® | cerebral contusion | ÇÑ±Û | ³úÁ»ó |
|---|---|---|---|
| ¼³¸í | ¿ÜºÎ¿¡¼ ±â¿øÇÏ´Â ¹°¸®Àû Ãæ°Ý¿¡ ÀÇÇÑ ³úÀÇ ¹°¸®Àû ¼Õ»ó. |
||
| ¿µ¹® | cerebral concussion | ÇÑ±Û | ³úÁøÅÁ |
|---|---|---|---|
| ¼³¸í | ¿ÜºÎ¿¡¼ ±â¿øÇÏ´Â ¹°¸®Àû Ãæ°ÝÀ¸·Î ÀÎÇØ ³úÀÇ ¹°¸®Àû ¼Õ»ó¾øÀÌ ÀϾ´Â ³úÀÇ ±â´É Àå¾Ö. ÀϽÃÀûÀ¸·Î ¹«ÀǽÄ, ¹Ý»ç¼Ò½Ç, µîÀÌ ³ªÅ¸³ªÁö¸¸ °á±¹Àº ¾Æ¹« ÈÄÀ¯Áõ¾øÀÌ Á¤»óÀ¸·Î µ¹¾Æ¿Â´Ù. |
||
| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
|---|---|
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| CM | California mastitis [test]; calmodulin; capreomycin; carboxymethyl; cardiac murmur; cardiac muscle; ... |
| CPC | central posterior curve; cerebellar Purkinje cell; cerebral palsy clinic; cerebral performance categ... |
| CT | calcitonin; calf testis; cardiac tamponade; cardiothoracic [ratio]; carotid tracing; carpal tunnel; ... |
| CBF | 1--Cerebral blood flow |
|---|---|
| ACA | Anterior Cerebral Artery |
| aCSF | Artificial cerebral spinal fluid |
| CADASIL | Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy |
| CBFv | Cerebral Blood Flow velocities |
| cerebral lipidosis | Any one of a group of inherited diseases characterised by failure to thrive, hypertonicity, progressive spastic paralysis, loss of vision and occurrence of blindness, usually with macular degeneration and optic atrophy, convulsions, and mental deterioration; associated with abnormal storage of sphingomyelin and related lipids in the brain. Four types are recognised as clinically and enzymatically distinct: 1) infantile type (Tay-Sachs disease, GM2 gangliosidosis) due to a deficiency of hexosaminidase A; 2) early juvenile type (Jansky-Bielschowsky or Bielschowsky's disease); 3) late juvenile type (Spielmeyer-Vogt disease; Spielmeyer-Sjogren disease; Batten-Mayou disease; ceroid lipofuscinosis); and 4) adult type (Kufs disease). Synonym: cerebral lipidosis. (05 Mar 2000) |
|---|
| ganglioside lipidosis | Any disease characterised, in part, by the abnormal accumulation within the nervous system of specific gangliosides, e.g., GM2 gangliosidosis, Tay-Sachs disease, caused by hexosaminidase A enzyme deficiency with accumulation of GM2 ganglioside Synonym: gangliosialidosis, ganglioside lipidosis. (05 Mar 2000) |
|---|---|
| glycolipid lipidosis | <disease> Lysosomal storage disease caused by a deficiency of alpha-galactosidase a and resulting in an accumulation of globotriaosylceramide in the renal and cardiovascular systems. The disease is characterised by telangiectatic skin lesions, renal failure, and disturbances of the cardiovascular, gastrointestinal, and central nervous systems. Inheritance: x-linked. (08 Mar 2000) |
| ceramide lactoside lipidosis | An inherited disorder associated with an accumulation of ceramide lactoside due to a deficiency of ceramide lactosidase; results in progressive brain damage with liver and spleen enlargement. (05 Mar 2000) |
| cerebroside lipidosis | <disease> A chronic congenital disease of lipid metabolism caused by a deficiency of the beta-glucocerebrosidase enzyme. The defect is most common in Ashkenazi Jews. Clinical features are hepatosplenomegaly (enlargement of liver and spleen) and in severe early onset forms of the disease, with neurological dysfunction. Inheritance: autosomal recessive. (27 Sep 1997) |
| sphingomyelin lipidosis | <disease> A family of severe lysosomal storage diseases resulting in an accumulation of sphingomyelin and other phospholipids in the reticuloendothelial system. The best studied forms are due to deficiency of sphingomyelinase and it is more common in Ashkenazi Jews than other groups. Clinical signs include foam cells in the blood and marrow, hepatosplenomegaly and neurologic degeneration. Diagnosis is confirmed by enzyme assay on leukocytes or fibroblasts and specific mutations in the gene are now recognised. (29 Dec 1997) |
| sulfatide lipidosis | <radiology> Dysmyelinating disease, autosomal recessive, aryl sulfatase A -- absent from urine and serum, most present by 2 yrs, die at 3-4 yrs, may arise at any age, CT: decreased density of white matter, primarily in centrum semiovale, with or without focal gall bladder defects (!) (12 Dec 1998) |
| lipidosis | Hereditary abnormality of lipid metabolism that results in abnormal amounts of lipid deposition; classification is typically based on the responsible enzymatic deficiency and type of lipid involved. Such enzymatic activity takes place in the lysosomes, and the abnormal products appear as lysosomal storage diseases. Sphingolipidoses make up the largest portion of recognised lipidoses, including abnormal metabolism of gangliosides, ceramides, and cerebrosides. Origin: Lipid + G. -osis, condition (05 Mar 2000) |
| anterior cerebral artery | <anatomy, artery> One of the two terminal branches (with middle cerebral artery) of the internal carotid; it passes anterior, loops around the genu of the corpus callosum then posteriorly in the interhemispheric fissure along with its fellow of the opposite side, the two being joined by the anterior communicating artery; for descriptive purposes it is divided into two parts: the precommunical part (A2 segment of clinical terminology), supplying branches to the thalamus and corpus striatum, and the postcommunical part, (A2) or pericallosal artery, supplying branches to the cortex of the medial parts of the frontal and parietal lobes. Synonym: arteria cerebri anterior. (05 Mar 2000) |
| anterior cerebral vein | <anatomy, vein> A small vein that parallels the anterior cerebral artery and drains into the basal vein. Synonym: vena cerebri anterior. (05 Mar 2000) |
| arteries of cerebral haemorrhage | Numerous small branches from the sphenoidal part of the middle cerebral arteries supplying the lateral and anterior parts of the corpus striatum. Synonym: arteriae centrales anterolaterales, arteriae thalamostriatae anterolaterales, anterolateral central arteries, anterolateral striate arteries, anterolateral thalamostriate arteries, arteries of cerebral haemorrhage, lenticulostriate arteries. (05 Mar 2000) |
| ganglionic layer of cerebral cortex | Layer 5 of the cortex cerebri. (05 Mar 2000) |
| malaria, cerebral | A condition that is most commonly seen as a severe complication of malaria, falciparum mainly involving the brain. It has also been reported to occur as a result of infection with other plasmodium species. This disease is often fatal and presents as disturbances in consciousness ranging from somnolence to coma, major motor seizures, and organic psychosis. The onset may be gradual or sudden following a convulsion. (12 Dec 1998) |
| ventricle of cerebral hemisphere | A cavity shaped somewhat like a horseshoe in conformity with the general shape of the hemisphere; each lateral ventricle communicates with the third ventricle through the interventricular foramen of Monro, and expands from there forward into the frontal lobe as the anterior horn as well as caudally over the thalamus as the central part or cella media which, behind the thalamus, curves ventrally and laterally, then forward into the temporal lobe as the inferior horn; from the apex of the curve a variably sized posterior horn extends back into the white matter of the occipital lobe. The large choroid plexus of the lateral ventricle invades the cella media and the inferior horn (but not the anterior and posterior horn) from the medial side. Synonym: ventriculus lateralis, ventricle of cerebral hemisphere. (05 Mar 2000) |
| paroxysmal cerebral dysrhythmia | A diffusely abnormal electroencephalogram often seen with epilepsy. (05 Mar 2000) |
| medial cerebral surface | It faces, above as well as anterior and posterior to the corpus callosum, the falx cerebri; below it are the mesencephalon and the dura-covered medial wall of the middle cranial fossa. Synonym: facies medialis cerebri, medial cerebral surface. (05 Mar 2000) |
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|