| 영문 | cerebral infarction | 한글 | 뇌경색증 |
|---|---|---|---|
| 설명 | 급격한 혈액 공급의 차단으로 인해서 조직이 죽는 것을 말한다. 뇌경색증은 뇌의 조직이 혈류의 급격한 차단에 의해서 죽은 것을 말한다. 혈류가 완전히 차단되면 국소에 혈액이 없어지므로 그 조직에 경색이 생기게 된다. 경색이 생긴 부위는 혈액의 공급이 없으므로 원칙적으로는 정상적으로 혈류가 공급되는 부위보다 창백하고 희게 보인다. 이런 부분을 백색경색(white infarct) 또는 빈혈경색(anemic infarct)라 한다. 하지만 이 부위에 이차적으로 적혈구가 빠져 들어가면 그 부위는 피가 고이게 되고 적색을 띠게 된다. 이런 부분을 적색경색(red infarct) 또는 출혈경색(hemorrhagic infarct)이라고 한다. 뇌의 경색증에는 이 두 가지 모두 발생가능하다. |
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| 영문 | cerebral aneurysm | 한글 | 뇌동맥류, 뇌동맥자루 |
|---|---|---|---|
| 설명 | 뇌의 동맥에 생긴 동맥자루. 임상적으로 중요시되는 이유는 이것이 잘 터져 뇌출혈의 중요한 원인이 되기 때문이다. 대부분의 동맥자루가 출혈을 일으키지만 출혈을 일으키지 않는 경우에는 주위의 뇌 조직의 압박에 의해서 두통이나 발작 등을 일으킬 수 있다. |
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| 영문 | cerebral palsy | 한글 | 뇌성마비 |
|---|---|---|---|
| 설명 | 출생전, 출생시 혹은 출생후의 뇌의 선천기형, 손상 혹은 중추신경계의 병에 의해서 영구적이며, 비진행성인 운동신경 및 정신장애를 일으키는 경우를 뜻한다. 원인은 여러 가지가 있을 수 있으나 조산으로 인한 뇌의 산소공급의 부족, 또는 난산으로 인한 호흡장애 등이 흔한 원인이다. 증상은 대개 비진행성의 뇌 병변으로 인한 운동장애가 대표적인 증상이며 그외에 청력, 시력의 장애, 지능부전, 언어장애, 경련 및 정신장애 등이 동반될 수 있다. |
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| 영문 | cerebral contusion | 한글 | 뇌좌상 |
|---|---|---|---|
| 설명 | 외부에서 기원하는 물리적 충격에 의한 뇌의 물리적 손상. |
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| 영문 | cerebral concussion | 한글 | 뇌진탕 |
|---|---|---|---|
| 설명 | 외부에서 기원하는 물리적 충격으로 인해 뇌의 물리적 손상없이 일어나는 뇌의 기능 장애. 일시적으로 무의식, 반사소실, 등이 나타나지만 결국은 아무 후유증없이 정상으로 돌아온다. |
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| GCL | globoid cell leukodystrophy |
|---|---|
| GLD | globoid leukodystrophy; glutamate dehydrogenase |
| MLD | manual lymph drainage; median lethal dose; metachromatic leukodystrophy; minimal lesion disease; min... |
| OLD | obstructive lung disease; orthochromatic leukodystrophy |
| PML | peripheral motor latency; polymorphonuclear leukocyte; posterior mitral leaflet; progressive multifo... |
| GLD | Globoid cell leukodystrophy |
|---|---|
| MLD | Metachromatic Leukodystrophy |
| HCHWA-D | Hereditary cerebral haemorrhage with amyloidosis, Dutch type |
| AHO | Albright hereditary osteodystrophy |
| CHED | Congenital Hereditary Endothelial Dystrophy |
| adrenal leukodystrophy | Sudanophilic leukodystrophy with bronzing of skin and adrenal atrophy. A metabolic disorder of young males, characterised by widespread myelin degeneration and associated adrenal insufficiency. The myelin degeneration is massive in various portions of the brain and sometimes the spinal cord, with the accumulation of degradation products of myelin in macrophages: sudanophilic demyelination; atrophy is present in the adrenal glands and testes, and markedly increased amounts of very long-chain fatty acid are present in both the brain and adrenal glands. Symptoms include bronzing of the skin, dysarthria, cortical blindness, bilateral hemiplegia, pseudobulbar paralysis, and progressive dementia. Probably sex-linked recessive inheritance. (05 Mar 2000) |
|---|---|
| globoid cell leukodystrophy | <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia Synonym: Krabbe leukodystrophy (12 Dec 1998) |
| metachromatic leukodystrophy | <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) |
| leukodystrophy | <radiology> Type of dysmyelinating disease, hereditary, peripheral nervous system unaffected in some disorders Specific diseases: adrenoleukodystrophy, metachromatic leukodystrophy, spongy degeneration (Canavan), globoid cell (Krabbe) leukodystrophy, Alexander disease, Pelizaeus-Merzbacher disease, Cockayne syndrome (12 Dec 1998) |
| leukodystrophy, globoid cell | An inherited metabolic disorder of the nervous system, particularly the white matter. It is characterised histologically by a paucity of myelin and oligodendroglia, severe astrocytic gliosis, and massive infiltration with unique multinucleated globoid cells which are enriched in galactosylceramide. The primary genetic defect is a deficiency of galactosylceramidase. (12 Dec 1998) |
| leukodystrophy, metachromatic | A sphingolipidosis where there is defective desulfation of galactosyl-3-sulfate ceramide due to a defective enzyme cerebroside sulfatase (arylsulfatase a). The result is an accumulation of sulfatide in neural and non-neural tissues which manifests as mental deterioration and severe disturbances of the central nervous system. (12 Dec 1998) |
| leukodystrophy with diffuse Rosenthal fibre formation | A metabolic disorder whose onset can be in infancy, adolescence, or adulthood; characterised pathologically by widespread cerebral demyelination with astrocyte and primitive oligodendroglial cell proliferation; refractile Rosenthal fibres result from the degeneration of these proliferating cells; aetiology unknown, but possibly due to a metabolic defect of astrocytes; sex-linked recessive disorder. (05 Mar 2000) |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |
| colourectal neoplasms, hereditary nonpolyposis | A syndrome characterised by autosomal dominant inheritance, a low mean age (41 years) for occurrence of colon cancer, and a marked increase in the proportion of tumours in the proximal colon. (12 Dec 1998) |
| corneal dystrophies, hereditary | Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect. (12 Dec 1998) |
| hereditary | <genetics> Transferred via genes from parent to child. (16 Dec 1997) |
| hereditary amyloidosis | <neurology> A disorder in which various peripheral nerves are infiltrated with amyloid and their functions disturbed, an abnormal prealbumin is also formed and is present in the blood; characteristically, it begins during mid-life and is found largely in persons of Portuguese descent. Other rare clinical types occur. Inheritance: autosomal dominant. Synonym: familial amyloidosis, hereditary amyloidosis. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|