| 영문 | histrionic personality disorder | 한글 | 히스테리인격장애 |
|---|---|---|---|
| 설명 | 지나치게 연극적이고 반응적이며 행동의 지나친 표현 및 특유한 대인관계의 장애를 주로 하는 정신병. 히스테리인격장애는 외부에 대한 반응이 지나치게 빠르고 자기를 과시하고 대인관계에서 피상적이고 불성실해서 대인관계에 장애가 있는 이상성격으로서 성심리가 미숙한 것이 특징이다. 언제나 자신을 멋지게 드러내 보이려 하고 다른 사람의 관심을 끌기 위해 과장된 표현을 한다. 아는 사람을 만나면 지나칠 정도로 반가워하고 마치 공주나 왕자같은 행세를 하는 수가 있다. 작은 자극에도 쉽게 흥분하고 화를 잘 내나 작은 기쁨에 지나치게 반응하는 변덕스러운 성격의 소유자이다. 논리적인 것보다는 감정적으로 일을 처리하고 대인관계에서 상대방의 의사를 자기 환상에 따라 멋대로 해석한다. 불만스러운 일이 있으면 자살한다고 위협하거나 자살의 연극을 꾸며서 상대방을 조정한다. 표면적으로는 감정이 풍부하고 매력적이고 사귀기 쉽지만 대인관계에서 지속성이 없고 쉽게 사귀었다가 쉽게 헤어지고 교제하는 사람은 많으나 상대가 자주 바뀐다. 한번 사귀게 되면 상대방의 의사는 아랑곳하지 않고 자기 요구만 들어주기를 바라는 이기적인 사람이고 그것이 충족되지 못하면 곧 실망하고 그 사람을 원망한다. 성적 적응력도 희박하여 성적으로 매력이 있어 보이고 애교가 있고 성적 분위기를 물씬 풍기지만 불감증인 경우가 많다. 이성관계를 낭만적인 환상으로 끌고 가려고 한다. |
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| HAE | health appraisal examination; hearing aid evaluation; hepatic artery embolism; hereditary angioneuro... |
|---|---|
| HANE | hereditary angioneurotic edema |
| HBC | hereditary breast cancer |
| HBOC | hereditary breast-ovarian cancer |
| HC | hair cell; hairy cell; handicapped; head circumference; head compression; health care; healthy contr... |
| spherocytosis, hereditary | A familial congenital haemolytic anaemia characterised by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions. (12 Dec 1998) |
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| neoplastic syndromes, hereditary | The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumour tends to occur at an earlier than average age, individuals may have more than one primary tumour, the tumours may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance. (12 Dec 1998) |
| nephritis, hereditary | Hereditary disease characterised initially by haematuria and slowly progressing to renal insufficiency. It is sometimes associated with perceptual deafness and/or congenital ocular defects. (12 Dec 1998) |
| neuropathies, hereditary motor and sensory | A group of slowly progressive inherited disorders in which the predominant involvement is the peripheral motor neurons with lesser involvement of the peripheral sensory neurons. Neuronal degeneration and atrophy are characteristic of these disorders. Some of the associated characteristics are phytanic acid excess, optic atrophy, and retinitis pigmentosa. (12 Dec 1998) |
| neuropathies, hereditary sensory and autonomic | A group of inherited disorders in which there is selective involvement of the peripheral sensory and autonomic neurons and degeneration of fibres by axonal atrophy and degeneration. Five types of disorders have been described and classified type I through type v. (12 Dec 1998) |
| oedema, hereditary angioneurotic | 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) |
| optic atrophy, hereditary | An inherited disorder in which optic atrophy is associated with muscle weakness, peroneal muscular atrophy and, in some patients, lancinating pains. In these patients the peripheral sensory neurons are probably affected. (12 Dec 1998) |
| telangiectasia, hereditary haemorrhagic | An autosomal dominant vascular anomaly characterised by the presence of multiple small telangiectases of the skin, mucous membranes, gastrointestinal tract, and other organs, associated with recurrent episodes of bleeding from affected sites and gross or occult melena. (12 Dec 1998) |
| elliptocytosis, hereditary | An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape. (12 Dec 1998) |
| exostoses, multiple hereditary | Hereditary disorder transmitted by an autosomal dominant gene and characterised by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation. (12 Dec 1998) |
| eye diseases, hereditary | Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder. (12 Dec 1998) |
| Leber's hereditary optic atrophy | Hereditary degeneration of the optic nerve and papillomacular bundle with resulting rapid loss of central vision, progressive for several weeks, then usually stationary with permanent central scotoma; age of onset is variable, most often in the third decade; more males than females are affected and transmission is cytoplasmic and strictly on the female side. Mutation on the mitochondrial chromosome involved, which presumably interacts with an X-linked mutant. This mechanism may explain the bizarre sex ratio, which differs significantly from one country to another. (05 Mar 2000) |
| affective personality disorder | A disturbance of feelings or mood expressed as a milder form of depression and related emotional features that colour the whole psychic life and for which psychosocial stressors are believed to play the major role. (05 Mar 2000) |
| alcohol amnestic disorder | <psychiatry> A mental disorder with brain damage characterised by amnesia, compensatory confabulation, disturbance of attention, and peripheral neuritis. It is usually associated with alcoholism and dietary deficiencies. (12 Dec 1998) |
| antisocial personality disorder | <psychiatry> An individual who engages in deviant behaviour with lack of remorse. (13 Jan 1998) |