| 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 | ceramide dihexoside; congenital diaphragmatic hernia; congenital dislocation of hip; congenital dysp... |
|---|---|
| AVF | 1) Arterio-Venous Fistula - Arterio-Venous Fistula 2) Augmented Voltage F... |
| VACTERL | vertebral abnormalities, anal atresia, cardiac abnormalities, tracheoesophageal fistula and/or esoph... |
| ACR | abnormally contracting region; absolute catabolic rate; acriflavine; adenomatosis of colon and rectu... |
| HACR | hereditary adenomatosis of the colon and rectum |
| artificial anus | An opening into the bowel, usually in the right or left flank, as a result of a colostomy. (05 Mar 2000) |
|---|---|
| Bartholin's anus | Entrance to the cerebral aqueduct (of Sylvius) from the caudal part of the third ventricle. Synonym: aditus ad aqueductum cerebri, Bartholin's anus, opening to cerebral aqueduct. (05 Mar 2000) |
| vesicalis anus | Imperforate anus with urinary bladder opening into the anus. (05 Mar 2000) |
| vestibular anus | <anatomy, surgery> A congenital malformation in which the anus is imperforate but the rectum opens into the vagina just above the vulva. (05 Mar 2000) |
| corrugator cutis muscle of anus | Smooth muscle fibres radiating from the anal opening superficial to the external sphincter. Synonym: musculus corrugator cutis ani. (05 Mar 2000) |
| imperforate anus | <embryology, paediatrics> A congenital obstruction of the anal opening. Occurs in approximately 1 in 5,000 infants. This condition is corrected through surgery. (27 Sep 1997) |
| internal sphincter muscle of anus | <anatomy> A smooth muscle ring, formed by an increase of the circular fibres of the rectum, situated at the upper end of the anal canal, internal to the outer voluntary external anal sphincter. This sphincter is maximally-contracted when the rectal ampulla is at rest -empty or relaxed to accommodate a distending faecal mass. It is inhibited with filling of the ampulla, increased distension and peristalsis. Synonym: musculus sphincter ani internus, internal sphincter muscle of anus. (05 Mar 2000) |
| elevator muscle of anus | <anatomy> Formed by pubococcygeus and iliococcygeus muscles; origin, posterior body of pubis, tendinous arch of the levator ani, and spine of ischium; insertion, anococcygeal ligament, sides of the lower part of the sacrum and of coccyx; action, resists prolapsing forces and draws the anus upward following defecation; supports the pelvic viscera; nerve supply, nerve to levator ani (fourth sacral spinal nerve). Synonym: musculus levator ani, elevator muscle of anus. (05 Mar 2000) |
| external sphincter muscle of anus | A fusiform ring of striated muscular fibres surrounding the anus, attached posteriorly to the coccyx and anteriorly to the central tendon of the perineum; it is subdivided, often indistinctly, into a subcutaneous part, a superficial part and a deep part for descriptive purposes. Synonym: musculus sphincter ani externus, external sphincter muscle of anus. (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) |