the Wilms Tumor 1 (WT1) or Wilms Tumor 2 (WT2) genes, and the tumor presents with a group of other signs and symptoms. Non-syndromic Wilms' tumor is not... 31 KB (2,961 words) - 03:04, 8 March 2024 |
syndrome (PS), also known as nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome, is a rare overgrowth syndrome caused by autosomal recessive... 8 KB (700 words) - 07:19, 15 April 2024 |
Wilms tumor-4 is a protein that in humans is encoded by the WT4 gene. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National... 361 bytes (41 words) - 06:18, 27 March 2022 |
Sidney Farber (section Wilms' tumor) treatment protocols by the National Wilms Tumor Study Group resulted in a 90% survival rate in children with Wilms' tumors by the end of the century. In 1939... 16 KB (1,720 words) - 10:30, 7 April 2024 |
Childhood cancer (redirect from Childhood Brain Tumors) atypical teratoid rhabdoid tumor. Other, less common childhood cancer types are: Neuroblastoma (6%, nervous system) Wilms tumor (5%, kidney) Non-Hodgkin... 55 KB (5,812 words) - 00:03, 22 April 2024 |
Denys–Drash syndrome (redirect from Wilms tumor and pseudohermaphroditism) and Wilms' tumor. Clinically, Denys–Drash is characterized by the triad of pseudohermaphroditism, mesangial renal sclerosis, and Wilms' tumor. The condition... 5 KB (468 words) - 04:26, 22 February 2023 |
WAGR syndrome (redirect from Wilms tumor-aniridia syndrome) WAGR syndrome (also known as WAGR complex, Wilms tumour-aniridia syndrome, aniridia-Wilms tumour syndrome) is a rare genetic syndrome in which affected... 9 KB (967 words) - 13:28, 12 March 2024 |
Beckwith–Wiedemann syndrome (category Syndromes with tumors) Omphalocele (also called exomphalos) or umbilical hernia Embryonal tumor (e.g., Wilms tumor, hepatoblastoma, neuroblastoma, rhabdomyosarcoma) in childhood... 31 KB (3,949 words) - 17:49, 23 January 2024 |
syndrome Williams syndrome Wilms' tumor Wilms tumor and pseudohermaphroditism Wilms tumor radial bilateral aplasia Wilms tumor-aniridia syndrome Wilson's... 5 KB (439 words) - 17:45, 14 March 2022 |
Johann Wilhelm Wilms (1772–1847), Dutch-German composer Max Wilms (1867–1918), German pathologist and surgeon Wilms' tumor, a rare tumor, most common in... 426 bytes (92 words) - 13:52, 23 May 2023 |
Intermediate mesoderm (section Wilm's tumor) and collecting duct of the adult kidney. Wilms' tumor (WT), also known as nephroblastoma, is an embryonic tumor originating from metanephric blastemal cells... 14 KB (1,553 words) - 00:40, 6 January 2024 |
National Wilms Tumor Study Group (NWTS) is a cancer research cooperative group in the United States formed to study a type of kidney tumor that affects... 2 KB (225 words) - 22:25, 15 March 2021 |
Malignant rhabdoid tumour (redirect from Rhabdoid tumor) variant of Wilms' tumour, which is primarily a kidney tumour that occurs mainly in children. MRT was first described as a variant of Wilms' tumour of... 9 KB (1,071 words) - 17:31, 3 December 2023 |
Virtual karyotype (section Wilms' tumor) R; Tomlinson G; Huff V; Green DM; National Wilms Tumor Study Group (October 2005). "National Wilms Tumor Study Group. Loss of heterozygosity for chromosomes... 61 KB (7,333 words) - 10:17, 28 November 2023 |
A sarcoma is a malignant tumor, a type of cancer that arises from cells of mesenchymal (connective tissue) origin. Connective tissue is a broad term that... 35 KB (3,903 words) - 02:28, 27 March 2024 |
Elevated alpha-fetoprotein (section Tumor marker) Sertoli-Leydig cell tumor, which itself is rare, rarely secretes AFP. In Wilms tumor AFP is rarely elevated, but when it is elevated it may serve as a marker... 17 KB (2,195 words) - 23:37, 7 November 2023 |
chemistry Wild type (wt), in genetics, denoting a control or unaltered form Wilms' tumor, a cancer of the kidneys that typically occurs in children Well tank... 3 KB (294 words) - 17:07, 28 March 2024 |
1007/s00277-013-1865-3. PMID 23925930. S2CID 12851937. Treatment of Wilms Tumor at National Cancer Institute. Last Modified: 03/29/2012 El Weshi, A;... 22 KB (562 words) - 06:39, 30 November 2023 |
Sertoli–Leydig cell tumour (redirect from Sertoli-Leydig cell tumor) may be a personal or family history of other rare tumors such as pleuropulmonary blastoma, Wilms tumor and cervical rhabdomyosarcoma. Closely related terms... 7 KB (703 words) - 09:37, 31 December 2023 |
Mesoblastic nephroma (section Tumor pathology) neoplasms: Wilms tumor is the most common childhood kidney neoplasm, representing some 85% of cases. Unlike mesoblastic nephroma, <2% of Wilms tumor patients... 18 KB (2,202 words) - 04:39, 31 March 2023 |
Pectus Excavatum Childhood tumors: like Neuroblastoma, Wilms' tumor, Rhabdomyosarcoma, ATRT, Liver tumors, Teratomas, kidney tumors: Separation of conjoined... 6 KB (562 words) - 08:45, 7 April 2024 |
medication used to treat a number of types of cancer. This includes Wilms tumor, rhabdomyosarcoma, Ewing's sarcoma, trophoblastic neoplasm, testicular... 20 KB (1,865 words) - 04:30, 3 January 2024 |
an increased risk for embryonal tumors, mainly Wilms tumor and hepatoblastoma. Due to the heightened tumor risk, a tumor screening protocol is recommended... 4 KB (541 words) - 19:34, 14 January 2024 |