| 영문 | narcissistic personality disorder | 한글 | 자기애적 인격장애 |
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| 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 | 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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| IA | ibotenic acid; immune adherence; immunoadsorbent; immunobiologic activity; impedance angle; indolami... |
|---|---|
| IAFI | infantile amaurotic familial idiocy |
| IBSN | infantile bilateral striated necrosis |
| ICP | incubation period; indwelling catheter program; infantile cerebral palsy; infection-control practiti... |
| IDBS | infantile diffuse brain sclerosis |
| infantile cortical hyperostosis | Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood. Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome. (05 Mar 2000) |
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| infantile digital fibromatosis | Multiple fibrous flesh-coloured nodules on the extensor aspect of the terminal phalanges of adjacent digits of infants and young children which often recur after attempted excision, do not metastasize, and may spontaneously regress in two to three years; composed of spindle cells containing cytoplasmic inclusions believed to be derived from myofibrils. Synonym: infantile digital fibromatosis. (05 Mar 2000) |
| infantile diplegia | A type of cerebral palsy in which there is bilateral spasticity, with the lower extremities more severely affected. Compare: flaccid paralysis. Synonym: Erb-Charcot disease, infantile diplegia, Little's disease, spastic spinal paralysis, tabes spasmodica. (05 Mar 2000) |
| infantile dwarfism | 1. A state marked by slow development of mind and body. Synonym: infantile dwarfism. 2. Childishness, as characterised by a temper tantrum of an adolescent or adult. 3. Underdevelopment of the sexual organs. (05 Mar 2000) |
| infantile eczema | Eczema in infants; the clinical appearance varies according to the dominant causative mechanism, e.g., contact-type hypersensitivity, candidiasis, atopy, seborrhoea, or a combination including intertrigo and diaper dermatitis. (05 Mar 2000) |
| infantile fibrosarcoma | <tumour> A rapidly growing but infrequently metastasizing fibrosarcoma which usually appears on the extremities in the first year of life. (05 Mar 2000) |
| infantile gastroenteritis | An endemic viral gastroenteritis of young children (6 months to 12 years) that is especially widespread during winter, caused by strains of rotavirus; the incubation period is 2 to 4 days, with symptoms lasting 3 to 5 days, including abdominal pain, diarrhoea, fever, and vomiting. Synonym: infantile gastroenteritis. (05 Mar 2000) |
| infantile gastroenteritis virus | <virology> Genus of the Reoviridae having a double layered capsid and 11 double stranded RNA molecules in the genome. They have a wheel like appearance in the electron microscope and cause acute diarrhoeal disease in their mammalian and avian hosts. Probably the most important cause of severe dehydrating diarrhoea in children under three years of age worldwide. Symptoms include nausea, vomiting, low-grade fever and diarrhoea. Aggressive fluid replacement is generally required. (27 Sep 1997) |
| infantile generalised GM1 gangliosidosis | One of the hereditary metabolic diseases of infancy; resembles Tay-Sachs disease, except other organ systems (bone, liver, kidney) are affected. Synonym: familial neuroviscerolipidosis, pseudo-Hurler disease, Type 1 GM1 gangliosidosis. (05 Mar 2000) |
| infantile GM2 gangliosidosis | <disease> A genetic disorder found in east European Jewish families which can result in early death bu affecting the brain and nerves by causing abnormal lipid metabolism. It is a lysosomal disease in which there is a deficiency of hexosaminidase A, an enzyme that degrades ganglioside GM2. Symptoms appear at age 3-6 months and include blindness, deafness, seizures, paralysis, dementia, decreased muscle tone and growth retardation. There is no known treatment and most children usually die between 2 and 5 years of age. Inheritance: autosomal recessive. (06 Oct 1997) |
| infantile hemiplegia | Indefinite term for any motor abnormality in the infant caused by or attributed to the birthing process; includes obstetrical paralysis, infantile hemiplegia, etc. Synonym: infantile hemiplegia. (05 Mar 2000) |
| infantile hernia | A hernia in which an intestinal loop descends behind the tunica vaginalis, having, therefore, three peritoneal layers in front of it. (05 Mar 2000) |
| infantile hydrocephalus | <radiology> A VP-Shunt Can Decompress The Hydrocephalic Child, Aqueductal stenosis, Vein of Galen aneurysm, Postinfectious, Superior vena cava obstruction, Chiari malformation, Dandy-Walker syndrome, Tumour, Haemorrhage, Choroid plexus papilloma see: hydrocephalus (12 Dec 1998) |
| infantile hypothyroidism | <paediatrics> Stunted body growth and mental development appearing in the first years of life resulting the inappropriate development of the thymus gland or inadequate maternal intake of iodine during gestation. (27 Sep 1997) |
| infantile leishmaniasis | Visceral leishmaniasis in infants, from Leishmania donovani infantum. (05 Mar 2000) |