| 영문 | myopia | 한글 | 근시 |
|---|---|---|---|
| 설명 | 시각을 형성하는 눈의 촛점이 망막보다 앞쪽에 맞추어져 가까이 있는 물체는 보이지만, 멀리 있는 물체가 잘 보이지 않는 현상. 정도에 따라 심한 경우 고도근시(high myopia)라 부르며, 이 경우에 여러 가지 합병증의 발생가능성이 높으며, 선천적인 경우가 많다. |
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| 영문 | nyctalopia, night blinduese | 한글 | 야맹증, 밤소경 |
|---|---|---|---|
| 설명 | 밤에 잘 보이지 않는 증상을 말함. 이런 증상은 주로 비타민 A의 결핍에서 잘 나타나지만, 때로는 유전적인 색소망막염에서도 볼 수 있다. |
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| 영문 | congenital syphilis | 한글 | 선천매독 |
|---|---|---|---|
| 설명 | 임부가 매독에 감염되어 있으면 임신 후기에 매독균이 태반을 통해 혈행성으로 태아에 감염(수직감염)된 것을 말하다. 대부분은 유산, 사산이 되지만 출생하면 제2기 이후의 발진을 보인다. 발현시기에 따라서 ① 태아매독, ② 유아매독, ③ 만발성 선천매독으로 분류된다. ①에서는 뼈연골염, 간-지라 비대와 매독성 천포창, ②에서는 파로가성마비와 매독성 코염, ③에서는 허친슨 세징후(허친슨 치아, 속귀성 난청, 실질성 각막염)에 따라 특징이 있다. 기타 수두증, 지능발육 불량 등을 자주 볼 수 있다. 매독 혈청반응은 대부분의 경우 양성으로 나온다. 매우 드물게 간세포내에서 매독균을 무수히 볼 수 있다. 간세포 주변의 섬유화와 함께 불규칙한 흉터(hepar lobatum)를 만들 수 있다. |
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| 영문 | congenital rubella syndrome | 한글 | 선천풍진증후군 |
|---|---|---|---|
| 설명 | 임신기간 중에 산모가 풍진에 걸리면 이 풍진 바이러스는 태반을 통해서 태아에게 전달되어서 태아의 풍진감염을 일으킨다. 임신 첫 3개월 동안, 특히 임신 첫달에 태아가 풍진의 감염을 받으면, 신생아에서 선천기형, 즉 눈에서 촛점을 정확히 맞추어주는 렌즈의 역할을 하는 수정체의 혼탁(백내장), 심장기형, 귀머거리 및 심한 지능박약을 동반하는 소두증 등이 발생하는 수가 많다. |
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| 영문 | congenital heart disease | 한글 | 선천심장병 |
|---|---|---|---|
| 설명 | 선천적으로 심장의 구조에 이상이 있는 병. |
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| CDH | 1) Chronic Daily Headache = CTH = ... |
|---|---|
| CDH | ceramide dihexoside; congenital diaphragmatic hernia; congenital dislocation of hip; congenital dysp... |
| Myop. | Myopia |
| Amh | mixed astigmatism with myopia predominating |
| IMPC | International Myopia Prevention Center |
| FDM | Form-deprivation myopia |
|---|---|
| CCHB | Complete congenital heart block |
| C.C.A.M. | Congenital Cystic Adenomatoid Malformation |
| CDH | Congenital Diaphragmatic Hernia |
| CDH | Congenital Dislocation of the Hip |
| nyctalopia | Night blindness or difficulty in seeing at night. Symptom of vitamin A deficiency. (27 Sep 1997) |
|---|---|
| malignant myopia | pathologic myopia |
| myopia | <ophthalmology> That error of refraction in which rays of light entering the eye parallel to the optic axis are brought to a focus in front of the retina, as a result of the eyeball being too long from front to back (axial myopia) or of an increased strength in refractive power of the media of the eye (index myopia). Also called nearsightedness, because the near point is less distant than it is in emmetropia with an equal amplitude of accommodation. Origin: Gr. Myein = to shut (18 Nov 1997) |
| senile lenticular myopia | 1. <ophthalmology> Improved near vision in the aged as a result of increased refractivity of the nucleus of the lens causing myopia. Synonym: senile lenticular myopia. 2. The power of discerning what is not visible to the physical eye, or of foreseeing future events. Such as are of a disastrous kind, the capacity of a seer or prophetic vision. Source: Websters Dictionary (01 Mar 1998) |
| simple myopia | Myopia arising from failure of correlation of the refractive power of the anterior segment and the length of the eyeball. Space myopia, a type of myopia arising when no contour is imaged on the retina. Transient myopia, myopia observed in accommodative spasm secondary to iridocyclitis or ocular contusion. (05 Mar 2000) |
| night myopia | In dark adaptation the eye becomes more sensitive to shorter wave lengths (Purkinje shift), and visual acuity depends on parafoveal blue cones. Shorter wavelengths come into focus in front of the retina, and this chromatic aberration accounts for some of the relative myopia that a normal eye experiences at night; much of the remainder is due to an increase in accommodative tone in the dark. Pathologic myopia, progressive myopia marked by fundus changes, posterior staphyloma, and subnormal corrected acuity. Synonym: degenerative myopia, malignant myopia. Prematurity myopia, myopia observed in infants of low birth weight or in association with retrolental fibroplasia. (05 Mar 2000) |
| degenerative myopia | pathologic myopia |
| index myopia | Myopia arising from increased refractivity of the lens, as in nuclear sclerosis. (05 Mar 2000) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
| bullous congenital ichthyosiform erythroderma | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
| pain insensitivity, congenital | Absence of sensibility to pain or inability to feel pain. The condition is present at birth. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|