Wilms tumor

To assess the results of surgical treatment of Wilms tumors in children according to SIOP 2001. Study method: A descriptive and retrospective study of cases diagnosed of Wilms tumors by age, ac-cording to Algorithm of Diagnosis and Treatment of Wilms Tumors (SIOP 2001).

7p vinatisu 29-08-2024 0 0   Download

Wilms tumor is a highly heritable malignancy. Aberrant METTL14, a critical component of N6-meth‑ yladenosine (m6 A) methyltransferase, is involved in carcinogenesis. The association between genetic variants in the METTL14 gene and Wilms tumor susceptibility remains to be fully elucidated.

10p vielonmusk 21-01-2022 20 0   Download

The impact of hepatic resection for liver metastases (LM) on the survival of pediatric patients with Wilms’ tumor (WT) is unclear. So far, there is a lack of studies investigating the best suited treatment for patients with WTLM, and the role of liver resection has rarely been investigated. Thus, the development of evidence-based guide‑ lines concerning indications of liver resection for WTLM remains difficult.

16p vielonmusk 21-01-2022 13 1   Download

Wilm’ Tumor (Nephroblastoma): Bướu thận ác, gặp ở trẻ 1- 6 tuổi, kèm không mống mắt bẩm sinh (Ahiridia), hemihypertrophy, tiểu máu vi thể, sốt, BC, cao HA (50%). Wilm’ tumor cả 2 bên: 10%

33p dell_12 27-06-2013 70 7   Download

Microdeletion Syndromes The term contiguous gene syndrome refers to genetic disorders that mimic a combination of single-gene disorders. They result from the deletion of a small number of tightly clustered genes. Because some are too small to be detected cytogenetically, they are termed microdeletions. The application of molecular techniques has led to the identification of at least 18 of these microdeletion syndromes (Table 63-4). Some of the more common ones include the Wilms' tumor–aniridia complex (WAGR), Miller Dieker syndrome (MDS), and velocardiofacial (VCF) syndrome.

5p konheokonmummim 03-12-2010 76 3   Download