## Abstract We report on a patient with WiedemannโBeckwith syndrome (WBS) who developed abdominal neuroblastoma. Although WBS patients are known to have a higher incidence of embryonal tumors, this is only the 4th known case of neuroblastoma associated with this syndrome. Chromosomes on peripheral
Medullary sponge kidneys and unilateral Wilms tumour in a child with Beckwith-Wiedemann syndrome
โ Scribed by R. Beetz; O. Schofer; H. Riedmiller; R. Schumacher; P. Gutjahr
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 787 KB
- Volume
- 150
- Category
- Article
- ISSN
- 0340-6997
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๐ SIMILAR VOLUMES
## Background: We undertook a cost-benefit analysis of screening for wilms tumor and hepatoblastoma in children with beckwith-wiedemann syndrome (bws), a known cancer predisposition syndrome. the purpose of this analysis was twofold: first, to assess whether screening in children with bws has the p
## Abstract To evaluate the usefulness of regular radiographic screening to detect an asymptomatic intraabdominal tumor in patients with an increased risk of developing Wilms tumor, we reviewed the files of patients with hemihypertrophy, aniridia, or BeckwithโWiedemann syndrome who were registered