| UNTS | unilateral nevoid telangiectasia syndrome |
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| MNBCCS | multiple nevoid basal-cell carcinoma syndrome |
| NBCC | nevoid basal cell carcinoma |
| NBCCS | nevoid basal cell carcinoma syndrome |
| NBS | N-bromosuccinimide; National Bureau of Standards; neuroblastoma supressor; nevoid basal cell carcino... |
| NBCCS | Nevoid Basal Cell Carcinoma Syndrome |
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| ATM | Ataxia Telangiectasia Mutated |
| HHT | Hereditary Haemorrhagic Telangiectasia |
| HHT1 | Hereditary Haemorrhagic Telangiectasia Type 1 |
| AUN | Acute unilateral nephrectomy |
telangiectasis
| nevoid | Resembling a nevus. Synonym: nevose, nevous. Origin: L. Naevus, mole (nevus), + G. Eidos, resemblance (05 Mar 2000) |
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| nevoid amentia | A familial disorder characterised by unilateral nevus, contralateral hemiplegia, hemianopia, cerebral angioma, and mental retardation; possibly a variant of Sturge-Weber syndrome. Synonym: nevoid amentia. (05 Mar 2000) |
| nevoid basal cell carcinoma syndrome | <syndrome> An inherited group of defects which involve abnormalities of the skin, eyes, nervous system, endocrine, glands and bones. The condition is characterised by an unusual facial appearance and a predisposition for skin cancer. (27 Sep 1997) |
| nevoid elephantiasis | Thickening of skin, usually unilateral, involving a small area or the entire extremity, due to congenital enlargement of lymph vessels and lymph vessel obstruction. (05 Mar 2000) |
| nevoid hypertrichosis | Congenital growth of hair abnormal for its site, texture, colour, or length; often associated with other nevoid abnormalities. (05 Mar 2000) |
| unilateral | <anatomy> Affecting only one side. Origin: L. Latus = side (18 Nov 1997) |
| unilateral anaesthesia | <neurology> The inability to feel touches (tactile sensations) on one side of the body. (09 Oct 1997) |
| unilateral hemianopia | Uniocular hemianopia, loss of sight in one-half of the visual field of one eye only. (05 Mar 2000) |
| unilateral hermaphroditism | Hermaphroditism in which the doubling of sex characteristics occurs on one side only: ovotestis on one side and either ovary or testis on the other. (05 Mar 2000) |
| unilateral hyperlucent lung | Chronic bronchiolitis obliterans predominating on one side. See: unilateral lobar emphysema. (05 Mar 2000) |
| unilateral large kidney | <radiology> Multifocal: xanthogranulomatous pyelonephritis (XGP), malakoplakia, multicystic dysplastic kidney Cf: other urographic patterns smooth kidney: renal vein thrombosis, acute arterial infarction, obstructive uropathy, acute bacterial nephritis, compensatory hypertrophy, duplicated pelvocalyceal system Cf: other urographic patterns multifocal: solid neoplastic mass, malignant, adenocarcinoma, adult nephroblastoma, invasive transitional cell carcinoma, sarcoma, metastasis, benign, hamartoma, adenoma, mesenchymal tumour cystic mass, simple cyst, focal hydronephrosis, multilocular cystic nephroma, arteriovenous malformation Cf: other urographic patterns (12 Dec 1998) |
| unilateral lobar emphysema | A state in which the roentgenographic density of one lung (or one lobe) is markedly less than the density of the other(s) because of the presence of air trapped during expiration. Synonym: Macleod's syndrome, Swyer-James syndrome. (05 Mar 2000) |
| unilateral rib notching | <radiology> Aortic coarctation, proximal to left subclavian artery most likely to be right, anomalous right subclavian artery most likely to be left, subclavian artery stenosis / atresia, most likely to be IPSIlateral, Blalock-Taussig shunt, anastamosis of subclavian artery to pulmonary artery, for Tetralogy of Fallot, most likely to be IPSIlateral (12 Dec 1998) |
| unilateral small kidney | <radiology> Scarred: reflux nephropathy, lobar infarction Cf: other urographic patterns smooth kidney: ischemia due to focal arterial disease, chronic infarction, radiation nephritis, congenital hypoplasia, post-obstructive atrophy, post-inflammatory atrophy, reflux atrophy Cf: other urographic patterns (12 Dec 1998) |
| ataxia-telangiectasia | <neurology, oncology> An intriguing autosomal recessive disorder in which a single defective gene produces myriad and protean effects, presents with cerebellar ataxia, telangiectasias in the eyes and skin, immune deficiency and autoimmune phenomena, propensity for lymphoid and other malignancies, excessive sensitivity to ionising radiation, increased serum alpha-fetoprotein concentrations and a tendency for chromosome breakage and translocation. A syndrome characterised by choreoathetosis beginning in childhood, progressive cerebellar ataxia, telangiectasis of conjunctiva and skin, slowly progressive mental deterioration and increasing cerebellar degeneration. There is evidence that heterozygotes show an increased susceptibility to malignancy as well, with breast cancer often cited. The gene was localised by linkage studies to chromosome 11q22-23, and recently cloned, revealing it to be homologous to the PI-3 kinase family so that prenatal diagnosis by RFLP analysis is possible. Other related genes are suspected to exist. Diagnosis in affected patients is made on clinical grounds, by detection of high concentrations of alpha-fetoprotein, and by a specialised cell culture assay for radiosensitivity and atypical radioresistant DNA synthesis. These cell culture methods are also used for prenatal diagnosis. A characteristic autopsy feature of ataxia-telangiectasia is the presence of empty basket cells in the cerebellum which results from degeneration of the previously contained Purkinje cells. Inheritance: autosomal recessive. (16 Dec 1998) |
| unilateral nevoid telangiectasia s. |
generalized essential telangiectasia representing a latent vascular nevus that becomes manifest under the possible influence of estrogens (pregnancy, menarche) or increased venous pressure (liver disease). Called also unilateral nevoid telangiectasia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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