| 영문 | eye | 한글 | 눈, 안구 |
|---|---|---|---|
| 설명 | 눈확 안에 박혀있는 공모양의 시각기관이다. 안구는 3층의 피막(공막)과 각막, 맥락막, 망막에 싸여 있다. 각각의 피막은 몇 개의 층으로 나누어진다. 3층의 피막 중에는 빛을 굴절하는 매체[방수, 수정체, 유리체액]이 있다. 외측의 공막은 백색이며 섬유상 조직이다. 공막부에서는 시각신경섬유가 채판의 작은구멍을 통해서 안구내로 들어간다. 공막의 내측 표면은 섬세한 결합조직과 갈색판에 의해서 맥락막과 접하고 있다. 각막은 5층이며, 그 내층은 장막으로서 데스메막이라 불리고 있다. 포도막은 주로 혈관과 색소로 되어 있다. 앞부는 수정체의 주변부로서 섬모체돌기라 불리는 주름의 형으로 끝난다. 망막은 주로 신경조직으로서 크게는 세개의 층으로 되어 있다. 외층막은 신경세포로 되어 있고 그 형상에 따라 원뿔체와 막대체로 불린다. 홍채는 중앙에 동공을 갖는 부분으로, 윤상과 방사상의 평활근섬유를 갖고 있다. 홍채의 색은 여러 가지이며, 수정체의 앞 방수중에 위치하고 있다. 섬모체인대는 홍채를 둘러싸고 있는 고리모양의 결합섬유이다. 섬유체근은 홍채의 주위를 둘러싸고, 조절할 때는 수정체의 형을 바꾼다. 방수는 전부의 각막과 후부의 수정체 사이에 있다. 유리체액은 수정체 후부의 공간을 채우며, 투명한 젤리상의 물질이고, 유리체막에 싸여 있다. 수정체는 유리체액과 방수의 사이에 있는 양쪽이 볼록한 투명한 물체로, 탄성피막과 소대인대에 의해서 알맞은 장소에 달려 있다. 눈의 동맥은 짧은 섬모체동맥, 긴섬모체동맥, 전섬모체동맥, 망막중심동맥 등이다. 신경은 시각신경, 긴섬모체신경, 짧은 섬모체 신경등이다. |
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| 영문 | pink eye | 한글 | 분홍색눈, 충혈안 |
|---|---|---|---|
| 설명 | 충혈된 눈을 부르는 말이다. 대개 결막염과 같은 뜻으로 쓰인다. 결막은 눈을 밖에서 관찰했을 때 눈동자를 제외한 희게 보이는 부분을 말한다. 여기에 염증이 생긴 것을 결막염이라 하는데 대개 바이러스감염에 의한다. 전염이 잘 되며, 특히 수영장 이용이 많은 여름에 유행한다. 대표적인 것으로 아폴로눈병, 유행성각결막염 등이 있다. 특징적인 증상은 충혈된 눈모양이며, 치료는 특별한 것이 없고 2차감염을 예방하고 저절로 나을 때까지 기다려야 한다. 대개 2주후면 낫는다. |
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| 영문 | venereal disease, sexually transmitted diseases | 한글 | 성병 |
|---|---|---|---|
| 설명 | 보편적으로 성교 또는 성기접촉에 의해 걸리는 접촉 전염병으로 매독, 임질, 무른궤양, 샅굴육아종 등을 말한다. 치료는 원인균에 따른 적절한 항생요법이다. |
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| 영문 | psychosomatic diseases | 한글 | 정신신체질환 |
|---|---|---|---|
| 설명 | 여러 가지 정신적인 원인에 의한 신체 증상을 특징으로 하는 정신질환과 신체 질환의 혼합형을 이르는 말로, 정신 질환의 여러 가지 증상이 신체 증상으로 발현되는 질환이다. 신체 증상은 여러 다양한 장기가 관여하거나 또는 한 장기만 관여한다. |
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| ICD | I-cell disease; immune complex disease; implantable cardioverter defibrillator; impulse-control diso... |
|---|---|
| AJKD | American Journal of Kidney Diseases |
| ICD | 1) International (statistical) Classification of Diseases, (injuries & causes of death)<... |
| STDs | Sexual Transmitted Diseases [Chap 88, HP 534-43] |
| AASK | African American Study of Kidney Diseases and Hypertension Pilot Study |
| AID | Auto-immune diseases |
|---|---|
| CVD | Collagen vascular diseases |
| CTD | Connective Tissue Diseases |
| GSD I | Glycogen storage diseases type I |
| HCD | Heavy chain diseases |
| 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) |
|---|
| 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) |
| hereditary angioedema | 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) |
| hereditary angioneurotic oedema | 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) |
| hereditary angio oedema | <biochemistry> Condition in which there seems to be uncontrolled production of C2 kinin because of a deficiency in C1 inhibitor levels. (18 Nov 1997) |
| hereditary areflexic dystasia | A rare autosomal dominant neurological disorder with many of the clinical features of hereditary hypertrophic sensorimotor polyneuropathy combined with an essential tremor. Synonym: hereditary areflexic dystasia. (05 Mar 2000) |
| hereditary ataxia | A simple autosomal recessive trait in fox terrier dogs that produces a progressive general ataxia. (05 Mar 2000) |
| hereditary benign intraepithelial dyskeratosis | An autosomal dominant condition consisting of white spongy lesions of the buccal mucosa, floor of the mouth, ventral lateral tongue, gingiva and palate. Transient gelatinous plaques form over the cornea, which may produce temporary blindness, hereditary benign intraepithelial dyskeratosis. Synonym: hereditary benign intraepithelial dyskeratosis. (05 Mar 2000) |
| hereditary cerebellar ataxia | A disease of later childhood and early adult life, marked by ataxic gait, hesitating and explosive speech, nystagmus, and sometimes optic neuritis. It probably comprises several distinct conditions with diverse patterns of inheritance. Collective term for a number of hereditary disorders in which cerebellar signs are the most prominent finding. (05 Mar 2000) |
Synonyms : Hereditary Eye Diseases, Disease, Hereditary Eye, Diseases, Hereditary Eye, Eye Disease, Hereditary, Hereditary Eye Disease
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|