Congenital hepatoblastoma and schizencephaly in an infant with Beckwith-Wiedemann syndrome
β Scribed by Worth, Laura L.; Slopis, John M.; Herzog, Cynthia E.
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 128 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0098-1532
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## Abstract We report on a patient with WiedemannβBeckwith 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
## Abstract BeckwithβWiedemann 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,