| 영문 | bipolar disorder | 한글 | 양극성 장애 |
|---|---|---|---|
| 설명 | 외부자극에 의해서 변화하지 않는 지속적인 마음의 상태인 기분(mood)에 이상이 있는 정동장애의 한 종류. 정동장애의 대표적인 질환으로는 외부의 자극에 관계없이 기분이 우울한 우울증(depression)과 지속적으로 외부의 자극에 관계없이 지속적으로 기분이 들뜨는 조증(mania)이 있다. 우울증과 조증이 주기적으로 반복이 되는 정신질환과 조증만 있고 우울증은 없는 경우를 모두 포함하는 개념이다. |
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| 영문 | language disorder | 한글 | 언어장애 |
|---|---|---|---|
| 설명 | 말을 바르게 발음하지 못하거나 정확하게 이해하지 못하는 병증. 교통수단으로서의 언어로 정보를 전달하는데 있어서의 장애이다. 언어를 이해, 표출하는 생리학적, 심리학적, 언어학적, 물리학적, 사회학적인 각 과정에서의 질병이나 장애로 인해 일어나며 그 원인이나 병태에 따라 구음장애, 말더듬, 음성장애, 언어발달지체, 청력장애, 선천기형 등 많은 질병, 장애로 세분된다. 원인 및 병태의 검사, 진단에는 내과, 이비인후과, 정신과, 치과 등 여러 과목에 걸쳐 정밀조사를 함과 동시에 언어기능검사를 해야 한다. |
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| 영문 | personality disorder | 한글 | 인격장애, 성격장애 |
|---|---|---|---|
| 설명 | 타고난 인성과 성장과정의 여러 사건, 그리고 교육정도에 따라 개인의 인격은 형성된다. 이런 인격(성격)이 사회생활, 혹은 가족생활에 지장을 주거나, 자기자신의 생활에 피해를 주는 경우, 이를 인격장애라 부른다. 실제로 이런 일련의 성격들은 누구나 정상적으로 나타날 수 있으나, 이상성격이 심한 경우 치료의 대상이 된다. |
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| 영문 | narcissistic personality disorder | 한글 | 자기애적 인격장애 |
|---|---|---|---|
| 설명 | 자신의 중요성과 독특함, 유일함에 대한 광적인 집착과 자신이 성공할 것이라는 지나친 집착을 보여주는 성격장애. 지나친 자기에의 만족감을 가지고, 지나친 자신감, 성공에 대한 확신을 지니고 있다. |
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| 영문 | conversion disorder | 한글 | 전환장애 |
|---|---|---|---|
| 설명 | 내부의 갈등에 대한 무의식적 방어메커니즘으로 내부의 갈등을 특정한 신체의 증상으로 변환하여 나타내는 것을 말 한다. 이 전환으로 인한 증상을 주로 나타내는 정신질환을 전환장애라고 한다. 전환으로 인한 증상으로 대표적인 것으로는 마비, 경련, 의식장애 등이다. 대개 그 병을 일으킬 만한 병변이 존재하지 않고, 심리적 갈등이 심할 경우에 더욱 증상이 심해지고 증상의 발현으로 인해서 내부적 갈등이 감소되고 증상의 발현으로 인한 2차적 이득(가족들의 관심집중, 돌봐줌)이 있는 것이 이 전환장애의 특징이다. 대개 이 전환장애 환자는 자신의 질환에 대해서 특징적으로 매우 무관심한 태도를 취한다. |
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| DD | dangerous drug; data definition; day of delivery; degenerated disc; degenerative disease; delusional... |
|---|---|
| PAD | pain and distress; patient surface axis depth; percutaneous abscess drainage; percutaneous automated... |
| SPD | schizotypal personality disorder; sociopathic personality disorder; specific paroxysmal discharge; s... |
| FAC | Familial Amyloid Cardiomyopathy |
| FAP | Familial Amyloid Polyneuropathy |
| Danubian endemic familial nephropathy | A tubulointerstitial disease of unknown aetiology occurring in a limited geographic area including adjacent regions of romania, bulgaria, and yugoslavia. (12 Dec 1998) |
|---|---|
| diffuse infantile familial sclerosis | <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia Synonym: Krabbe leukodystrophy (12 Dec 1998) |
| dysautonomia, familial | An autosomal recessive inherited disorder seen predominantly in jewish infants and children. The peripheral autonomic and sensory neurons are affected. The characteristic distinguishing this disorder from other hereditary sensory and autonomic neuropathies is the predominance of autonomic symptoms such as excessive perspiration, defective lacrimation, and hypertension. Insensitivity to pain and areflexia are also present. (12 Dec 1998) |
| type I familial hyperlipoproteinaemia | Hyperlipoproteinaemia characterised by the presence of large amounts of chylomicrons and triglycerides in the plasma when the patient has a normal diet, and their disappearance on a fat-free diet; low alpha-and beta-lipoproteins on a normal diet, with increase on fat-free diet; decreased plasma postheparin lipolytic activity; and low tissue lipoprotein lipase activity. It is accompanied by bouts of abdominal pain, hepatosplenomegaly, pancreatitis, and eruptive xanthomas; autosomal recessive inheritance. See: familial lipoprotein lipase inhibitor. Synonym: Burger-Grutz syndrome, familial fat-induced hyperlipaemia, familial hyperchylomicronaemia, familial hypertriglyceridemia, idiopathic hyperlipaemia. (05 Mar 2000) |
| type II familial hyperlipoproteinaemia | Hyperlipoproteinaemia characterised by increased plasma levels of beta-lipoproteins, cholesterol, and phospholipids, but normal triglycerides; heterozygotes have mild lipid changes and are susceptible to atherosclerosis in middle age, but homozygotes have severe changes often with generalised xanthomatosis and xanthelasma, and frank clinical atherosclerosis as young adults. The primary defect is a deficiency of apoprotein of VLDL, and the disorder is divided into two classes: 1) type IIA, which has elevated LDL due to a deficiency of the receptor or a modified apolipoprotein B-100; 2) type IIB, which has elevated LDL and triglycerides; autosomal dominant inheritance. Synonym: familial hyperbetalipoproteinaemia, familial hypercholesteraemic xanthomatosis, familial hypercholesterolaemia. (05 Mar 2000) |
| type III familial hyperlipoproteinaemia | Hyperlipoproteinaemia characterised by increased plasma levels of LDL, beta-lipoproteins, pre-beta-lipoproteins, cholesterol, phospholipids, and triglycerides; hypertriglyceridemia induced by a high carbohydrate diet, and glucose tolerance is abnormal; frequent eruptive xanthomas and atheromatosis, particularly coronary artery disease; biochemical defect lies in apolipoproteins; there are many varieties. Synonym: carbohydrate-induced hyperlipaemia, dysbetalipoproteinaemia, familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia, familial hypercholesterolaemia with hyperlipaemia. (05 Mar 2000) |
| type IV familial hyperlipoproteinaemia | Plasma levels of VLDL, pre-beta-lipoproteins and triglycerides are increased on a normal diet, but beta-lipoproteins, cholesterol, and phospholipids are normal; hypertriglyceridemia is induced by a high carbohydrate diet; may be accompanied by abnormal glucose tolerance and susceptibility to ischemic heart disease; probably autosomal recessive inheritance. Synonym: carbohydrate-induced hyperlipaemia, familial hyperprebetalipoproteinaemia, familial hypertriglyceridemia. (05 Mar 2000) |
| type V familial hyperlipoproteinaemia | Hyperlipoproteinaemia characterised by increased plasma levels of chylomicrons, VLDL, pre-beta-lipoproteins, and triglycerides, and slight rise of cholesterol on a normal diet, with beta-lipoproteins normal; may be accompanied by bouts of abdominal pain, hepatosplenomegaly, susceptibility to atherosclerosis, and abnormal glucose tolerance; probably autosomal recessive inheritance. Synonym: combined fat-and carbohydrate-induced hyperlipaemia, familial hyperchylomicronaemia with hyperprebetalipoproteinaemia, mixed hyperlipaemia. (05 Mar 2000) |
| familial | Occurring in families. An inherited disorder or trait. (27 Sep 1997) |
| familial adenomatous polyposis | <gastroenterology> Genetic disease with numerous precancerous polyps in the colon and rectum. Also called familial polyposis. (12 Dec 1998) |
| familial aggregation | <genetics> The occurrence of a trait in more members of a family than can be readily accounted for by chance; presumptive but not cogent evidence of the operation of genetic factors. (05 Mar 2000) |
| familial amyloid neuropathy | <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) |
| familial 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) |
| familial aortic ectasia | <cardiology, syndrome> The concurrence as an autosomal dominant trait of bicuspid aortic valve often with premature calcification, ectasia and dissection of the aorta and, rarely, coarctation of the aorta. Superficially resembles the Marfan's syndrome. Synonym: familial aortic ectasia. (05 Mar 2000) |
| familial aortic ectasia syndrome | <cardiology, syndrome> The concurrence as an autosomal dominant trait of bicuspid aortic valve often with premature calcification, ectasia and dissection of the aorta and, rarely, coarctation of the aorta. Superficially resembles the Marfan's syndrome. Synonym: familial aortic ectasia. (05 Mar 2000) |