Wiedemann-Beckwith syndrome: Further prenatal characterization of the condition
β Scribed by Reish, Orit ;Lerer, Israela ;Amiel, Aliza ;Heyman, Eli ;Herman, Arie ;Dolfin, Tzipora ;Abeliovich, Dvorah
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 109 KB
- Volume
- 107
- Category
- Article
- ISSN
- 0148-7299
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π SIMILAR VOLUMES
We report a case of congenital pancreatic cyst detected prenatally by ultrasound in a fetus with evidence for a diagnosis of Beckwith-Wiedemann syndrome (BWS). Neonatal hypoglycaemia was prevented. The cyst was managed by internal drainage. This is the second reported case of BWS associated with pan
Beckwith-Wiedemann syndrome (BWS) comprises of a number of childhood abnormalities, often associated with one or more tumors. Thirty-eight patients were investigated to determine clinical and/or biological signs associated with a tumor presence. Our patients exhibited a higher incidence of tumor dev
## INAUGURAL DR. ClULlO 1. D'ANGIO AWARD of adults who have been both cured of their tumor and In 1940, the diagnosis of Wilms' tumor was associated with the same poor prognosis as that of other forms of childhood cancer. The addition of radiation therapy, and then chemotherapy to the management