| ¿µ¹® | senile dementia | ÇÑ±Û | ³ëÀÎÄ¡¸Å |
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| ¿µ¹® | dementia | ÇÑ±Û | Ä¡¸Å |
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| 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. |
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| ACA | abnormal coronary artery; acrodermatitis chronica atrophicans; acute cerebellar ataxia; adenocarcino... |
|---|---|
| CLA | cerebellar ataxia; Certified Laboratory Assistant; cervicolinguoaxial; contralateral local anesthesi... |
| COACH | cerebellar vermis hypoplasia/aplasia-oligophrenia-congenital ataxia-ocular colobomata-hepatic fibros... |
| EOCA | early onset cerebellar ataxia |
| SCA | self-care agency; severe congenital anomaly; sickle-cell anemia; single-camera autostereoscopic [ima... |
| ADCA | Autosomal Dominant Cerebellar Ataxia |
|---|---|
| AT | Ataxia Telangiectasis |
| ATM | Ataxia Telangiectasia Mutated |
| FA | Friedreich ataxia |
| FRDA | Friedreich ataxia |
| cerebellar ataxia | Loss of muscle coordination caused by disorders of the cerebellum. (05 Mar 2000) |
|---|---|
| hereditary cerebellar ataxia | A disease of later childhood and early adult life, marked by ataxic gait, hesitating and explosive speech, nystagmus, and sometimes optic neuritis. It probably comprises several distinct conditions with diverse patterns of inheritance. Collective term for a number of hereditary disorders in which cerebellar signs are the most prominent finding. (05 Mar 2000) |
| primary progressive cerebellar degeneration | A familial ataxic condition related to cerebellar degeneration. (05 Mar 2000) |
| progressive cerebellar tremor | <syndrome> An intention tremor beginning in one extremity, gradually increasing in intensity, and subsequently involving other parts of the body. Synonym: progressive cerebellar tremor. Facial paralysis, otalgia, and herpes zoster resulting from viral infection of the seventh cranial nerve and geniculate ganglion, a form of juvenile paralysis agitans associated with primary atrophy of the pallidal system. Synonym: paleostriatal syndrome, pallidal syndrome. Synonym: Ramsay Hunt's syndrome. (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) |
| secondary dementia | Chronic dementia following and due to a psychosis or some other underlying disease process. Senile dementia, dementia of Alzheimer's disease developing after age 65. Toxic dementia, dementia caused by an exogenous agent. (05 Mar 2000) |
| senile dementia | <neurology> A form of dementia caused by destruction (atrophy) of the frontal lobes of the brain. This condition leads to the progressive deterioration of mental functioning. Incidence: 9 out of 10,000 people in the population. (27 Sep 1997) |
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