๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Neuroblastoma in a patient with the Beckwith-Wiedemann syndrome (BWS)

โœ Scribed by Yoon, Grace ;Graham, Gail ;Weksberg, Rosanna ;Gaul, H. Penney ;DeBaun, Michael R. ;Coppes, Max J.


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
104 KB
Volume
38
Category
Article
ISSN
0098-1532

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Neuroblastoma in a child with Wiedemann-
โœ Chitayat, David ;Friedman, J. M. ;Dimmick, James E. ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 445 KB ๐Ÿ‘ 3 views

## Abstract We report on a patient with Wiedemannโ€Beckwith 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

Atypical teratoid/rhabdoid tumor in a pa
โœ Eric M. Jackson; Tamim H. Shaikh; Fan Zhang; Luanne M. Wainwright; Phillip B. St ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 101 KB ๐Ÿ‘ 3 views

## Abstract Beckwithโ€“Wiedemann syndrome (BWS) is a genetic disorder associated with an increased risk of childhood tumors. Here we describe a patient with BWS who developed a central nervous system atypical teratoid/rhabdoid tumor (AT/RT). To our knowledge, despite the known cancer predisposition,