| 영문 | Wilms' tumor | 한글 | 윌름즈종양 |
|---|---|---|---|
| 설명 | 콩팥에서 발생하는 악성종양으로 소아에서 자주 발생한다. 흔히 소아에서 복부내종양을 발견시 중앙선을 넘어서면 신경모세포종이고, 중앙선을 넘지 않으면 윌름즈종양을 의심할 만큼 중요하고 흔한 종양이다. 대개 증상은 없는 편이며, 주로 아기의 목욕을 시켜주다가 우연히 발견된 복부내종괴 때문에 병원을 찾게 된다. 진단시 컴퓨터단층촬영으로 주위의 전이가 없는지를 확인해야 하며, 전이가 없으면 항암화학요법, 방사선치료요법, 그리고 수술요법의 병합요법에 의한 치료효과가 높다. |
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| WAGR syndrome | Wilms's Tumor Aniridia Genital Anomalies Me... |
|---|---|
| AWTA | aniridia-Wilms tumor association |
| NWTS | National Wilms' Tumor Study |
| WAGR | Wilms tumor, aniridia, genitourinary abnormalities, and mental retardation |
| WT | wall thickness; water temperature; wavelet transform; wild type [strain]; Wilms tumor; wisdom teeth;... |
| WT1 | Wilms tumour |
|---|---|
| NWTS | National Wilms Tumor Study |
| WT-1 | Wilms' Tumor-1 |
| ISG | IFN stimulated genes |
| mdr | Multidrug resistance genes |
| genes, wilms' tumour | Tumour suppressor genes located in the 11p13 region on the short arm of human chromosome 11. The absence of these genes is associated with the formation of wilms' tumour. (12 Dec 1998) |
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| wilms tumour | <radiology> Nephroblastoma, 3rd most common kiddie tumour (most common abdominal tumour), arises from embryonal renal tissue (nephroblastomatosis), large, only 10% are calcified, 4-10% bilateral, metastasis may lead to lungs, para-aortic nodes associated with: aniridia, Beckwith-Wiedemann syndrome, hemihypertrophy, Drash syndrome Cf: neuroblastoma (more likely calcified) (12 Dec 1998) |
|---|---|
| Wilms' tumour | A malignant renal tumour of young children, composed of small spindle cells and various other types of tissue, including tubules and, in some cases, structures resembling foetal glomeruli, and striated muscle and cartilage. Often inherited as an autosomal dominant trait . Synonym: adenomyosarcoma, embryoma of the kidney, nephroblastoma. (05 Mar 2000) |
| Wilms, Max | <person> German surgeon, 1867-1918. See: Wilms' tumour. (05 Mar 2000) |
| genes, suppressor, tumour | Genes that inhibit expression of the tumourigenic phenotype. They are normally involved in holding cellular growth in check. When tumour suppressor genes are inactivated or lost, a barrier to normal proliferation is removed and deregulated growth is possible. (12 Dec 1998) |
| breast cancer susceptibility genes | Inherited factors that predispose to breast cancer. Put otherwise, these genes make one more susceptible to the disease and so increase the risk of developing breast cancer. Two of these genes, BRCA1 and BRCA2, have been identified (and prominently publicised). Several other genes (those for the Li-Fraumeni syndrome, Cowden disease, Muir-Torre syndrome, and ataxia-telangiectasia) are also known to predispose to breast cancer. However, since all of these known breast cancer susceptibility genes together do not account for more than a minor fraction (1/5th at most) of breast cancer that clusters in families, it is clear that more breast cancer genes remain to be discovered. (12 Dec 1998) |
| cancer, breast, susceptibility genes | Inherited factors that predispose to breast cancer. Put otherwise, these genes make one more susceptible to the disease and so increase the risk of developing breast cancer. Two of these genes, BRCA1 and BRCA2, have been identified (and prominently publicised). Several other genes (those for the Li-Fraumeni syndrome, Cowden disease, Muir-Torre syndrome, and ataxia-telangiectasia) are also known to predispose to breast cancer. However, since all of these known breast cancer susceptibility genes together do not account for more than a minor fraction (1/5th at most) of breast cancer that clusters in families, it is clear that more breast cancer genes remain to be discovered. (12 Dec 1998) |
| genes | Located in the nucleus of the cell, genes contain hereditary information that is transferred from cell to cell. (09 Oct 1997) |
| genes, abl | Retrovirus-associated DNA sequences (abl) originally isolated from the abelson murine leukaemia virus (ab-mulv). The proto-oncogene abl (c-abl) codes for a protein that is a member of the tyrosine kinase family. The human c-abl gene is located at 9q34.1 on the long arm of chromosome 9. It is activated by translocation to bcr on chromosome 22 in chronic myelogenous leukaemia. (12 Dec 1998) |
| genes, apc | Tumour suppressor genes located in the 5q21 region on the long arm of chromosome 5. The mutation of these genes is associated with familial adenomatous polyposis (apc stands for adenomatous polyposis coli) and gardner's syndrome, as well as some sporadic colourectal cancers. (12 Dec 1998) |
| genes, arac | Regulatory genes which encode a cyclic AMP receptor protein required for l-arabinose utilization in e. Coli. It is an example of positive control or regulation of gene expression in the bacterial operon. (12 Dec 1998) |
| genes, archaeal | The genetic material of archaea. (12 Dec 1998) |
| genes, bacterial | The genetic material of bacteria. (12 Dec 1998) |
| genes, bcl-1 | The B-cell leukaemia/lymphoma-1 genes, associated with various neoplasms when overexpressed. Overexpression results from the t(11;14) translocation, which is characteristic of mantle zone-derived B-cell lymphomas. The human c-bcl-1 gene is located at 11q13 on the long arm of chromosome 18. (12 Dec 1998) |
| genes, bcl-2 | The B-cell leukaemia/lymphoma-2 genes, responsible for blocking apoptosis in normal cells, and associated with follicular lymphoma when overexpressed. Overexpression results from the t(14;18) translocation. The human c-bcl-2 gene is located at 18q24 on the long arm of chromosome 18. (12 Dec 1998) |
| genes, BRCA1 | Tumour suppressor genes located on human chromosome 17q12-21. The mutation of these genes is associated with the formation of familial breast and ovarian cancer. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|