| 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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| 영문 | affective disorder | 한글 | 정동장애 |
|---|---|---|---|
| 설명 | 주로 기분의 장애가 주축이 되는 일련의 정신장애이다. 이 병의 범주에는(우울병－지속적으로 우울한 기분이 외부자극과 관계없이 나타나는 병), (조병－지속적으로 들뜬 기분이 외부자극과 관계없이 계속되는 병) 등이 포함된다. |
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| 영문 | psychiatric disorder(s) | 한글 | 정신질환 |
|---|---|---|---|
| 설명 | 정신상태에 이상이 있는 질환으로, 정신분열병, 정동장애, 인격장애 등이 있다. |
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| 영문 | learning disorder | 한글 | 학습장애 |
|---|---|---|---|
| 설명 | 지능은 정상이지만 듣기, 말하기, 읽기, 쓰기, 추리 또는 계산능력에 심각한 문제가 나타나는 여러 장애들을 일컫는 용어. 이로 인해 학업성적 및 자신감 저하, 대인관계에서도 사교 능력이 미숙하여 일상생활의 모든 면에서 문제가 나타난다. 성인기 사회적응력에도 영향을 미칠 수 있으며, 행동장애, 주의력결핍, 과잉운동장애, 우울장애 등과 동반되어 나타날 수 있다. 그 유병률은 낮게는 1.7%, 높게는 30% 정도로 추정하고 있지만 학동기 아동의 약 3~9%가 이 장애를 갖고 있는 것으로 알려져 있다. 기초학습기능검사를 통하여 진단한다. 학습의 기회나 교육적인 자극이 부족한 경우, 집중력 부족, 우울증-불안 등 정서적 문제, 신경학적 이상에 의한 경우 등이 원인일 수 있다. 학습과 관련이 있는 뇌기능과 연관된 특정영역에 결함이 있거나 발육지연 또는 장애가 있는 경우도 원인이 된다. 또한 부모가 조기에 자녀의 능력과 적성을 잘 알지 못하는 경우에도 많이 생긴다. |
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| BCE | basal cell epithelioma; benign childhood epilepsy; bubble chamber equipment |
|---|---|
| BFEC | benign focal epilepsy of childhood |
| BPEC | benign partial epilepsy of childhood; bipolar electrocardiogram |
| CARS | Childhood Autism Rating Scale; Children's Affective Rating Scale; cysteinyl-transfer ribonucleic aci... |
| CCD | calibration curve data; central core disease; charge-coupled device; childhood celiac disease; cleid... |
omemtulum
Omenns syndrome : 동의어=histiocytic medullary reticulosis.
omental
| epithelial attachment | A collar of epthelial cells attached to the tooth surface and subepithelial connective tissue found at the base of the gingival crevice. Synonym: epithelial attachment. (05 Mar 2000) |
|---|---|
| key attachment | A frictional or mechanically retained unit used in fixed or removable prosthodontics, consisting of closely fitting male and female parts, an attachment that may be rigid in function or may incorporate a movable stress control unit to reduce the torque on the abutment. Synonym: frictional attachment, internal attachment, key attachment, keyway attachment, parallel attachment, slotted attachment. (05 Mar 2000) |
| keyway attachment | A frictional or mechanically retained unit used in fixed or removable prosthodontics, consisting of closely fitting male and female parts, an attachment that may be rigid in function or may incorporate a movable stress control unit to reduce the torque on the abutment. Synonym: frictional attachment, internal attachment, key attachment, keyway attachment, parallel attachment, slotted attachment. (05 Mar 2000) |
| frictional attachment | A frictional or mechanically retained unit used in fixed or removable prosthodontics, consisting of closely fitting male and female parts, an attachment that may be rigid in function or may incorporate a movable stress control unit to reduce the torque on the abutment. Synonym: frictional attachment, internal attachment, key attachment, keyway attachment, parallel attachment, slotted attachment. (05 Mar 2000) |
| benign childhood epilepsy with centrotemporal spikes | A specific epilepsy syndrome beginning in childhood and remitting in adolescence, characterised by nocturnal simple partial motor seizures or generalised tonic-clonic seizures. EEG shows centrotemporal spikes that are activated by sleep and an otherwise normal EEG background. (05 Mar 2000) |
| papular acrodermatitis of childhood | <syndrome> A cutaneous manifestation of hepatitis B infection occurring in young children; an exanthem comprised of dusky papules on the legs, buttocks, and extensors of the arms; it lasts 2 to 8 weeks and is associated with adenopathy and malaise. Synonym: papular acrodermatitis of childhood. (05 Mar 2000) |
| recurrent pneumonia in childhood | <radiology> IMMUNE PROBLEMS, immune deficiency, chronic granulomatous disease of childhood, alpha-1 antitrypsin deficiency, ASPIRATION, GE reflux, H-type TE fistula, disorder of swallowing, oesophageal obstruction, UNDERLYING LUNG DISEASE, sequestration, brochopulmonary dysplasia, cystic fibrosis, atopic asthma, bronchiolitis obliterans, sinusitis, bronchiectasis, ciliary dysmotility syndromes, pulmonary foreign body (12 Dec 1998) |
| recurring digital fibromas of childhood | 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) |
| mental disorders diagnosed in childhood | Those psychiatric disorders usually first diagnosed in infancy, childhood, or adolescence. These disorders can also be first diagnosed during other life stages. (12 Dec 1998) |
| childhood | The period of life between infancy and puberty. (05 Mar 2000) |
| childhood absence epilepsy | A generalised epilepsy syndrome characterised by the onset of absence seizures in childhood, typically at age six or seven years. There is a strong genetic predisposition and girls are affected more often than boys. EEG reveals generalised 3 Hz spike-wave activity on a normal background. Prognosis for remission is good if the patient does not also have generalised tonic-clonic seizures. See: absence. Synonym: petit mal epilepsy, pyknolepsy. (05 Mar 2000) |
| childhood epilepsy with occipital paroxysms | A benign epilepsy syndrome characterised by frequent occipital spikes often activated by eye closure. It has a seizure semiology that includes visual manifestations; not always remitting later in life. (05 Mar 2000) |
| childhood muscular dystrophy | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |
| childhood schizophrenia | A severe emotional disturbance of childhood characterised by qualitative impairment in reciprocal social interaction and in communication, language, and social development. Synonym: autistic disorder, childhood schizophrenia, early infantile autism, Kanner's syndrome. (05 Mar 2000) |
| childhood tuberculosis | Initial (primary) infection with Mycobacterium tuberculosis, characterised by pneumonic lesions in middle parts of lungs, rarely cavitary, with rapid spread to lymph nodes in hilar and paratracheal areas; more often seen in childhood, but pattern is not limited to children. (05 Mar 2000) |