| 영문 | Alzheimer's disease | 한글 | 알츠하이머병 |
|---|---|---|---|
| 설명 | 퇴행성 뇌병. 노인에서의 치매의 원인 중 가장 흔한 형태이다. 병리조직학적으로는 뇌의 전반적인 위축, 뇌실의 확장, 신경섬유의 다발성 병터(신경섬유뒤틀림)와 노인반(neuritic plaque) 등이 특징이다. 임상적인 특징은 점진적인 기억-판단-언어능력 등 지적인 기능의 감퇴와 일상생활능력-인격-행동양상의 장애이다. 병에 걸리면 초기에는 이름-날짜-장소와 같은 것들이 기억에서 사라지고, 심해지면 화장실을 가거나 요리를 하거나 신을 신는 일 등의 일상생활조차도 잊게 된다. 동시에 우울증세나 인격의 황폐, 격한 행동 등의 정신의학적인 증세도 동반된다. 이러한 증세들이 점전적으로 진행되어 결국은 죽음에 이르게 된다. 발병 후 서서히 죽음에 이르는 기간은 6~8년 정도이지만 사람에 따라 20년이 넘는 경우도 있다. |
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| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
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| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| TAPVR | Total Anomalous Pulmonary Venous Return = TAPVC 4 Types of TAPVR &... |
| AD | accident dispensary; acetate dialysis; active disease; acute dermatomyositis; addict, addiction; ade... |
| ALL | Acute Lymphocytic Leukemia 형태학적 분류 L1; Small, Homogenous(... |
| O-2A | Oligodendrocyte-type 2 astrocyte |
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| ACM | Astrocyte conditioned medium |
| ATD | Alzheimer Type Dementia |
| AD | Alzheimer type dementia |
| D.A.T. | Dementia of Alzheimer Type |
| Alzheimer type I astrocyte | Enlarged frequently multinucleated astrocytes, seen in progressive multifocal leukoencephalopathy. (05 Mar 2000) |
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| Alzheimer type II astrocyte | Enlarged astrocytes with vesicular nuclei and one or more small basophilic nucleoli, seen in hepatocerebral disease and Wilson's disease. (05 Mar 2000) |
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| type 2 astrocyte | <pathology> A glial cell found in vertebrate brain, named for its characteristic star like shape. Astrocytes lend both mechanical and metabolic support for neurons, regulating the environment in which they function. See: oligodendrocytes. (18 Nov 1997) |
| Alzheimer, Alois | <person> In 1901 a 51 year old woman, Auguste D, was admitted to the state asylum in Frankfurt. She was suffering from cognitive and language deficits, auditory hallucinations, delusions, paranoia and aggressive behaviour. She was studied by Alzheimer who was working at the hospital in Frankfurt. He moved to the medical school in Munich in 1903, to work with Emil Kraepelin, one of the formost German psychiatrists of that era. When Auguste D died in April 1906, her brain was sent to him for examination. In November 1906, Alzheimer presented her case at a psychiatry meeting and published his talk in 1907. In 1910, Kraepelin coined the term Alzheimer's disease - a term still in use today. Lived: 1864-1915. (05 Dec 1998) |
| alzheimer disease | A degenerative organic mental disease characterised by progressive brain deterioration and dementia. The disease was originally described as dementia, presenile occurring in persons under the age of 65 (as opposed to dementia, senile with onset at or after 65); however, onset may occur at any age. There is no pathophysiological nor clinical distinction between the two stages of onset of alzheimer's. Women appear to be affected twice as frequently as men. It is characterised pathologically by the triad of senile plaques, neurofibrillary tangles, and neuropil threads. (12 Dec 1998) |
| 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) |
| Alzheimer's disease | <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) |
| Alzheimer's sclerosis | Hyaline degeneration of the medium and smaller blood vessels of the brain. (05 Mar 2000) |
| disease, alzheimer's | A progressive degenerative disease of the brain that leads to dementia. On a cellular level, Alzheimer's is characterised by unusual helical protein filaments in nerve cells (neurons) of the brain. These odd twisted filaments are called neurofibrillary tangles. On a functional level, there is degeneration of the cortical regions, especially the frontal and temporal lobes, of the brain. The U.S. President Ronald Reagan is said to have Alzheimer's disease. Named after the German neurologist Alois Alzheimer (1864-1915). (12 Dec 1998) |
| astrocyte | <pathology> A glial cell found in vertebrate brain, named for its characteristic star like shape. Astrocytes lend both mechanical and metabolic support for neurons, regulating the environment in which they function. See: oligodendrocytes. (18 Nov 1997) |
| Cajal's astrocyte stain | <technique> A method for demonstrating astrocytes by impregnation in a solution containing gold chloride and mercuric chloride. (05 Mar 2000) |
| gemistocytic astrocyte | <cell biology> A round to oval astrocyte cell with abundant cytoplasm containing glial filaments and an eccentric nucleus; may contain two nuclei in the cell hypertrophy of astrocytes. Synonym: gemistocyte, gemistocytic cell, reactive astrocyte, reactive cell. (05 Mar 2000) |
| reactive astrocyte | <cell biology> A round to oval astrocyte cell with abundant cytoplasm containing glial filaments and an eccentric nucleus; may contain two nuclei in the cell hypertrophy of astrocytes. Synonym: gemistocyte, gemistocytic cell, reactive astrocyte, reactive cell. (05 Mar 2000) |
| protoplasmic astrocyte | One form of astrocyte, found mainly in gray matter, having few fibrils and numerous branching processes. (05 Mar 2000) |
| fibrous astrocyte | Stellate astrocytic cell with long processes found mainly in the white matter of the brain and spinal cord and characterised by having bundles of glial filaments in its cytoplasm; origin of most astrocytomas. (05 Mar 2000) |
| acrocephalosyndactyly type 1 | <paediatrics> An inherited disease (autosomal dominant) or a spontaneously occurring disease characterised by a peaked head and unusual facial appearance, due to the premature closure of the cranial sutures. A skull X-ray can confirm the diagnosis and treatment is surgical. Inheritance: autosomal dominant. (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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