| 영문 | senile dementia | 한글 | 노인치매 |
|---|---|---|---|
| 설명 | 노화에 따른 뇌의 퇴행성 변화의 결과 나타나는 노인성 정신장애. 주로 지능의 기능저하로 일어나는데, 65세 전후부터 70세의 노년기에 일어나는 경우를 말한다. 생리적인 노인치매의 이행에 대해서는 현상적으로 명확한 구별을 할 수 없다. 노인성 변화로는 육안으로는 특히 이마엽에서 현저한 뇌의 위축을 볼 수 있으며, 조직학적으로는 신경세포의 감소, 신경세포 내의 리포프스친 증가, 노인반의 출현, 신경원섬유의 비후 등을 들 수 있다. 증세로는 심한 건망증과 기억장애로 시작하여 그런 장애를 얼버무리기 위한 말만들기 또는 지각저하가 생기고, 사고면에서는 군소리를 늘어놓거나 의욕만 앞서면, 판단력이나 추리력이 저하되고, 생산적 사고가 소실되며, 계산력이 쇠퇴하고, 사태에 대한 판단이 불가능해지는 등의 증세가 나타난다. |
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| 영문 | dementia | 한글 | 치매 |
|---|---|---|---|
| 설명 | 뇌의 기질적 장애에 의하여 후천적으로 일어나는 회복불능의 지능장애로서, 의식장애에 의한 것이 아닌 것을 말한다. 지능, 의지, 기억 등 정신적인 능력이 두드러지게 감퇴한 상태로서 정신박약과 같은 지능 장애인데, 정신박약이 주로 지능발육이 지체되거나 정지된 것인 데 비하여 치매는 일단 발달된 지능이 대뇌의 질환으로 인해 지속적으로 저하된 상태라는 점에서 구별된다. 과거의 체험에 의한 기억이나 지식이 단편적으로 남아 있고, 전체적으로 일정하지 않은 지능장애가 나타난다. |
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| 영문 | infectious disease | 한글 | 감염병 |
|---|---|---|---|
| 설명 | 바이러스로부터 기생충 크기까지의 생물을 원인으로 하는 병. 원인은 접촉전염성이며, 병원에서 감염되는 경우도 있다. 감염을 원인균에 따라 분류하면 바이러스, 세균, 클라미디아, 리켓차, 미코박테리움, 곰팡이, 원충, 윤충, 외부기생충 감염으로 나눌 수 있다. |
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| 영문 | hypertensive heart disease | 한글 | 고혈압심장병 |
|---|---|---|---|
| 설명 | 고혈압에 의해서 생기는 심장병. 고혈압심장병이라는 진단을 붙이기 위해서는 최소한 다음과 같은 조건이 부합되어야 하는데, 첫째 심장혈관계에 심장병을 유발할 수 있을 만한 다른 병변이 없이 좌심실 비대가 있어야 하며, 둘째 고혈압을 앓았다는 병력이 있어야 한다. 주로 고혈압에 의한 심장병은 초기에는 좌심실이 비후라는 것으로 특징되어진다. 즉 혈압이 높으므로 혈액을 순환시키기 위해서는 그만큼 심장의 혈액을 보내는 힘이 좋아야 한다. 그 힘을 얻기위해서는 심근의 비후가 필요로 하여 좌심실 근육의 비후가 생긴다. 그리고 고혈압이 지속이 될 경우에는 결국 심장이 제 구실을 하지 못하고 펌프로서의 기능을 잃어버리게 되어 심장기능상실에 빠지게 된다. |
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| 영문 | pelvic inflammatory disease | 한글 | 골반염질환 |
|---|---|---|---|
| 설명 | 골반주위의 장기에 발생하는 염증을 말함. 주로 여성에서 발생하며 원인은 임균(gonococcus)과 비임균에 의한 감염(non-gonorrheal infection)에 의한다. 증상은 초기에는 질분비물, 하복부동통, 여성의 생식기부위에 발생하는 압통, 월경통, 월경량의 증가 등이다. 일찍 치료해야 하며, 계속적으로 병이 지속시 여성의 불임의 원인이 된다. 후진국에서는 가장 많은 여성불임의 원인이기도 함. 치료는 항생제의 투여이다. |
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| HD | Haab-Dimmer [syndrome]; Hajna-Damon [broth]; Hansen disease; hearing distance; heart disease; helix ... |
|---|---|
| AD | accident dispensary; acetate dialysis; active disease; acute dermatomyositis; addict, addiction; ade... |
| PD | Doctor of Pharmacy; Dublin Pharmacopoeia; interpupillary distance; Paget disease; pancreatic duct; p... |
| CD | cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise... |
| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
| UHDRS | Unified Huntington Disease Rating Scale |
|---|---|
| HC | Huntington chorea |
| MID | 6-multiinfarct dementia |
| ADC | AIDS dementia complex |
| AD | Alzheimer Dementia |
Kugelberg-Welander disease 근 위축증의 유전성 연소형으로서 보통 상염색체성 열성 형질로 유전된다. 척수 전각의 병변이 그 원인이다.
kukuruku 원인 불명이며, 나이지리아에서 볼 수 있는 질환으로, 열
| Huntington disease | <neurology> An inherited adult-onset disease of the central nervous system. It is characterised by dementia and bizarre involuntary movements. The disease is progressive and there is currently no known cure. The identification of the gene (huntingtin) on chromosome 4p now allows for direct mutation analysis. The gene contains a trinucleotide repeat (CAG) that is found to be expanded in length in affected patients. The normal allele size ranges from 11 to 34 triplet repeat units, while 42 repeats or greater is considered diagnostic of Huntington disease. As in other trinucleotide repeat disorders, the phenomenom of anticipation has been observed, in this case expressed as earlier age of onset in offspring, particularly with paternal transmission. A further complication is the presence of two neighboring trinucleotide repeats (both CCG) which can expand independently without causing the disease. Early PCR primer sets encompassed these adjacent repeats, potentially yielding false positive test results, newer primers hone in more closely on the CAG repeat sequence. Careful attention must be paid to the psychosocial support structure of prospective test subjects in Huntington disease genetic counseling. Established protocols require systematic neuropsychiatric assessment and informed consent prior to DNA testing. Inheritance: autosomal dominant. (29 Dec 1997) |
|---|---|
| huntington's disease | An hereditary disorder with mental and physical deterioration leading to death. Although characterised as an adult-onset disease (as is usually the case), we have seen children with full-blown huntington's disease. (12 Dec 1998) |
| disease, huntington's | An hereditary disorder with mental and physical deterioration leading to death. Although characterised as an adult-onset disease (as is usually the case), we have seen children with full-blown Huntington's disease. (12 Dec 1998) |
| Huntington | George, U.S. Physician, 1850-1916. See: Huntington's chorea, Huntington's disease. (05 Mar 2000) |
| Huntington chorea | <neurology> An inherited adult-onset disease of the central nervous system. It is characterised by dementia and bizarre involuntary movements. The disease is progressive and there is currently no known cure. The identification of the gene (huntingtin) on chromosome 4p now allows for direct mutation analysis. The gene contains a trinucleotide repeat (CAG) that is found to be expanded in length in affected patients. The normal allele size ranges from 11 to 34 triplet repeat units, while 42 repeats or greater is considered diagnostic of Huntington disease. As in other trinucleotide repeat disorders, the phenomenom of anticipation has been observed, in this case expressed as earlier age of onset in offspring, particularly with paternal transmission. A further complication is the presence of two neighboring trinucleotide repeats (both CCG) which can expand independently without causing the disease. Early PCR primer sets encompassed these adjacent repeats, potentially yielding false positive test results, newer primers hone in more closely on the CAG repeat sequence. Careful attention must be paid to the psychosocial support structure of prospective test subjects in Huntington disease genetic counseling. Established protocols require systematic neuropsychiatric assessment and informed consent prior to DNA testing. Inheritance: autosomal dominant. (29 Dec 1997) |
| Huntington's chorea | A progressive disorder usually beginning in young to middle age, consisting of a triad of choreoathetosis, dementia, and autosomal dominant inheritance with complete penetrance. Bilateral marked wasting of the putamen and the head of the caudate nucleus is characteristic. Synonym: chronic progressive chorea, degenerative chorea, hereditary chorea, Huntington's disease. (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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|