| ¿µ¹® | senile dementia | ÇÑ±Û | ³ëÀÎÄ¡¸Å |
|---|---|---|---|
| ¼³¸í | ³ëÈ¿¡ µû¸¥ ³úÀÇ ÅðÇ༺ º¯ÈÀÇ °á°ú ³ªÅ¸³ª´Â ³ëÀμº Á¤½ÅÀå¾Ö. ÁÖ·Î Áö´ÉÀÇ ±â´ÉÀúÇÏ·Î ÀϾ´Âµ¥, 65¼¼ ÀüÈĺÎÅÍ 70¼¼ÀÇ ³ë³â±â¿¡ ÀϾ´Â °æ¿ì¸¦ ¸»ÇÑ´Ù. »ý¸®ÀûÀÎ ³ëÀÎÄ¡¸ÅÀÇ ÀÌÇà¿¡ ´ëÇØ¼´Â Çö»óÀûÀ¸·Î ¸íÈ®ÇÑ ±¸º°À» ÇÒ ¼ö ¾ø´Ù. ³ëÀμº º¯È·Î´Â À°¾ÈÀ¸·Î´Â ƯÈ÷ À̸¶¿±¿¡¼ ÇöÀúÇÑ ³úÀÇ À§ÃàÀ» º¼ ¼ö ÀÖÀ¸¸ç, Á¶Á÷ÇÐÀûÀ¸·Î´Â ½Å°æ¼¼Æ÷ÀÇ °¨¼Ò, ½Å°æ¼¼Æ÷ ³»ÀÇ ¸®Æ÷ÇÁ½ºÄ£ Áõ°¡, ³ëÀιÝÀÇ ÃâÇö, ½Å°æ¿ø¼¶À¯ÀÇ ºñÈÄ µîÀ» µé ¼ö ÀÖ´Ù. Áõ¼¼·Î´Â ½ÉÇÑ °Ç¸ÁÁõ°ú ±â¾ïÀå¾Ö·Î ½ÃÀÛÇÏ¿© ±×·± Àå¾Ö¸¦ ¾ó¹ö¹«¸®±â À§ÇÑ ¸»¸¸µé±â ¶Ç´Â Áö°¢ÀúÇϰ¡ »ý±â°í, »ç°í¸é¿¡¼´Â ±º¼Ò¸®¸¦ ´Ã¾î³õ°Å³ª Àǿ常 ¾Õ¼¸é, ÆÇ´Ü·ÂÀ̳ª Ã߸®·ÂÀÌ ÀúÇϵǰí, »ý»êÀû »ç°í°¡ ¼Ò½ÇµÇ¸ç, °è»ê·ÂÀÌ ¼èÅðÇϰí, »çÅ¿¡ ´ëÇÑ ÆÇ´ÜÀÌ ºÒ°¡´ÉÇØÁö´Â µîÀÇ Áõ¼¼°¡ ³ªÅ¸³´Ù. |
||
| ¿µ¹® | dementia | ÇÑ±Û | Ä¡¸Å |
|---|---|---|---|
| ¼³¸í | ³úÀÇ ±âÁúÀû Àå¾Ö¿¡ ÀÇÇÏ¿© ÈÄõÀûÀ¸·Î ÀϾ´Â ȸº¹ºÒ´ÉÀÇ Áö´ÉÀå¾Ö·Î¼, ÀǽÄÀå¾Ö¿¡ ÀÇÇÑ °ÍÀÌ ¾Æ´Ñ °ÍÀ» ¸»ÇÑ´Ù. Áö´É, ÀÇÁö, ±â¾ï µî Á¤½ÅÀûÀÎ ´É·ÂÀÌ µÎµå·¯Áö°Ô °¨ÅðÇÑ »óÅ·μ Á¤½Å¹Ú¾à°ú °°Àº Áö´É Àå¾ÖÀε¥, Á¤½Å¹Ú¾àÀÌ ÁÖ·Î Áö´É¹ßÀ°ÀÌ ÁöüµÇ°Å³ª Á¤ÁöµÈ °ÍÀÎ µ¥ ºñÇÏ¿© Ä¡¸Å´Â ÀÏ´Ü ¹ß´ÞµÈ Áö´ÉÀÌ ´ë³úÀÇ ÁúȯÀ¸·Î ÀÎÇØ Áö¼ÓÀûÀ¸·Î ÀúÇÏµÈ »óŶó´Â Á¡¿¡¼ ±¸º°µÈ´Ù. °ú°ÅÀÇ Ã¼Çè¿¡ ÀÇÇÑ ±â¾ïÀ̳ª Áö½ÄÀÌ ´ÜÆíÀûÀ¸·Î ³²¾Æ ÀÖ°í, ÀüüÀûÀ¸·Î ÀÏÁ¤ÇÏÁö ¾ÊÀº Áö´ÉÀå¾Ö°¡ ³ªÅ¸³´Ù. |
||
| DP | data processing; deep pulse; definitive procedure; degradation product; degree of polymerization; de... |
|---|---|
| MID | maximum inhibiting dilution; mesioincisodistal; midinfarct dementia; minimum infective dose; minimum... |
| MERRF Syndrome | Myoclonic Epilepsy & Ragged Red Fibers Syndrome |
| MTA | malignant teratoma, anaplastic; medical technical assistant; medical technology assessment; metatars... |
| SME | severe myoclonic epilepsy |
| JME | Juvenile Myoclonic Epilepsy |
|---|---|
| MERRF | Myoclonic Epilepsy and Ragged Red Fibers |
| MERRF | Myoclonic epilepsy with ragged-red fibers |
| PME | Progressive myoclonic epilepsy |
| SMEI | Severe myoclonic epilepsy in infancy |
| myoclonic | Showing myoclonus. (05 Mar 2000) |
|---|---|
| myoclonic astatic epilepsy | A petit mal variant characterised by atonic (drop attacks) and tonic or tonic-clonic attacks in neurologically disabled (hemiplegic, ataxic, etc.) children with mental retardation; characterised in EEG by 2/sec spike and wave discharges; usually progresses in spite of medication. (05 Mar 2000) |
| myoclonic seizure | Seizure associated with single or repetitive myoclonic jerks. (05 Mar 2000) |
| epilepsy, myoclonic | A progressive encephalopathy characterised by myoclonic jerks (single or repetitive muscle contractions involving one body part or the entire body), mental retardation, and ataxia. The disease, an autosomal recessive form of epilepsy, occurs usually at puberty. The most significant pathological findings are lafora's inclusion bodies, which contain mucopolysaccharides. (12 Dec 1998) |
| epilepsy with myoclonic absences | A form of generalised epilepsy characterised by absence seizures, severe bilateral rhythmic clonic jerks often associated with tonic contraction, and an EEG 3 Hz spike and wave pattern. Age of onset is usually around seven years and males are more often affected. (05 Mar 2000) |
| juvenile myoclonic epilepsy | An epilepsy syndrome typically beginning in early adolescence, and characterised by early morning myoclonic jerks that may progress into a generalised tonic-clonic seizure. A genetic disorder: some families have had gene linkage to chromosome-6. The EEG is characterised by generalised polyspike and wave discharges at 4-6 Hz. (05 Mar 2000) |
| AIDS dementia | <immunology> A frequent cerebral condition in people with AIDS that results in the loss of cognitive capacity, affecting the ability to function in a social or occupational setting. Its cause has not been determined exactly, but may result from HIV infection of cells in the brain or an inflammatory reaction to such infection. (09 Oct 1997) |
| AIDS dementia complex | <immunology> A frequent cerebral condition in people with AIDS that results in the loss of cognitive capacity, affecting the ability to function in a social or occupational setting. Its cause has not been determined exactly, but may result from HIV infection of cells in the brain or an inflammatory reaction to such infection. (09 Oct 1997) |
| Alzheimer's dementia | <disease> A progressive, neurodegenerative disease characterised by loss of function and death of nerve cells in several areas of the brain leading to loss of cognitive function such as memory and language. The cause of nerve cell death is unknown but the cells are recognised by the appearance of unusual helical protein filaments in the nerve cells (neurofibrillary tangles) and by degeneration in cortical regions of brain, especially frontal and temporal lobes. Alzheimer's disease is the most common cause of dementia. (22 May 1997) |
| vascular dementia | A state of diminished cognition that is the results from repeated cerebral strokes with a step-like deterioration in intellectual functions with focal neurological signs, as the result of multiple infarctions of the cerebral hemispheres. Synonym: multi-infarct dementia. (07 Mar 2000) |
| paralytic dementia | Dementia and paralysis resulting from a chronic syphilitic meningoencephalitis. Synonym: dementia paralytica. (05 Mar 2000) |
| catatonic dementia | Dementia with catatonic symptoms. (05 Mar 2000) |
| multi-infarct dementia | <neurology> This form of dementia is caused by a number of strokes in the brain. These strokes can cause specific symptoms, depending on their severity and location and can cause general symptoms of dementia. MID cannot be treated, once the nerve cells die, they cannot be replaced. However, the underlying condition leading to strokes (for example, high blood pressure, diabetes) can be treated, which may help prevent further damage. Synonym: vascular dementia. (22 May 1997) |
| presenile dementia | Dementia of Alzheimer's disease developing before age 65. Synonym: Alzheimer's disease. Primary dementia, dementia occurring independently as a mental disorder. (05 Mar 2000) |
| primary senile dementia | <disease> A progressive, neurodegenerative disease characterised by loss of function and death of nerve cells in several areas of the brain leading to loss of cognitive function such as memory and language. The cause of nerve cell death is unknown but the cells are recognised by the appearance of unusual helical protein filaments in the nerve cells (neurofibrillary tangles) and by degeneration in cortical regions of brain, especially frontal and temporal lobes. Alzheimer's disease is the most common cause of dementia. (22 May 1997) |
| myoclonic dementia |
dementia myoclo
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
|---|
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¿© |
|---|