| 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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| ABCDES | abnormal alignment, bones-periarticular osteoporosis, cartilage-joint space loss, deformities, margi... |
|---|---|
| CDH | 1) Chronic Daily Headache = CTH = ... |
| CDH | ceramide dihexoside; congenital diaphragmatic hernia; congenital dislocation of hip; congenital dysp... |
| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| FSW | feet of sea water |
|---|---|
| CCHB | Complete congenital heart block |
| C.C.A.M. | Congenital Cystic Adenomatoid Malformation |
| CDH | Congenital Diaphragmatic Hernia |
| CDH | Congenital Dislocation of the Hip |
| foot deformities, congenital | Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth. (12 Dec 1998) |
|---|---|
| limb deformities, congenital | Congenital structural deformities of the upper and lower extremities collectively or unspecified. (12 Dec 1998) |
| board feet | (BF) Unit of measure for logs and lumber. One board foot is equivalent to a piece of wood 1 inch thick, 12 inches wide, and 12 inches long. (05 Dec 1998) |
| sweaty feet syndrome | A disorder of leucine metabolism characterised by the excessive production of isovaleric acid upon protein ingestion or during infectious episodes; severe metabolic acidosis results from the large quantities of acid formed; autosomal recessive inheritance; due to a deficiency of isovaleryl-CoA dehydrogenase. Synonym: sweaty feet syndrome. (05 Mar 2000) |
| end-feet | The somewhat enlarged, often club-shaped endings by which axons make synaptic contacts with other nerve cells or with effector cells (muscle or gland cells). As isolated, by homogenizing brain or spinal cord, they contain acetylcholine and the related enzymes. Terminals contain neurotransmitters of various kinds, sometimes more than one. These can be demonstrated by chemical analysis and immunocytochemical methods. See: synapse. Synonym: axonal terminal boutons, end-feet, neuropodia, pieds terminaux, synaptic boutons, synaptic endings, synaptic terminals, terminal boutons, bouton terminaux. (05 Mar 2000) |
| feet | As a measure of length, the plural of foot. See Foot. (12 Dec 1998) |
| flat feet | All babies have flat feet because their arches are not yet built up (anf their feet tend to be plump). (12 Dec 1998) |
| hand deformities | Alterations or deviations from normal shape or size which result in a disfigurement of the hand. These can be acquired after birth as the result of injury or disease or congenital occurring at or before birth. (06 Mar 2000) |
| nose deformities, acquired | Deformities of the nose acquired after birth from injury or disease. (12 Dec 1998) |
| ear deformities, acquired | Distortion or disfigurement of the ear caused by disease or injury after birth. (12 Dec 1998) |
| joint deformities, acquired | Deformities acquired after birth as the result of injury or disease. The joint deformity is often associated with rheumatoid arthritis and leprosy. (12 Dec 1998) |
| foot deformities | Alterations or deviations from normal shape or size which result in a disfigurement of the foot. (12 Dec 1998) |
| foot deformities, acquired | Distortion or disfigurement of the foot, or a part of the foot, acquired through disease or injury after birth. (12 Dec 1998) |
| 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|