𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Experience with hemihyperplasia and Beckwith–Wiedemann syndrome surveillance protocol

✍ Scribed by Yuri A. Zarate; Rafael Mena; Lisa J. Martin; Paul Steele; Bradley T. Tinkle; Robert J. Hopkin

Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
210 KB
Volume
149A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Neuroblastoma in a child with Wiedemann-
Neuroblastoma in a child with Wiedemann-Beckwith syndrome
✍ Chitayat, David ;Friedman, J. M. ;Dimmick, James E. 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 445 KB 👁 2 views

## Abstract We report on a patient with Wiedemann‐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
Atypical teratoid/rhabdoid tumor in a patient with Beckwith–Wiedemann syndrome
✍ Eric M. Jackson; Tamim H. Shaikh; Fan Zhang; Luanne M. Wainwright; Phillip B. St 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 101 KB 👁 2 views

## Abstract Beckwith–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,