𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Prenatal diagnosis of the Beckwith-Wiedemann syndrome

✍ Scribed by Winter, Susan C. ;Curry, Cynthia J. R. ;Smith, J. Charles ;Kassel, Stephen ;Miller, Linda ;Andrea, Janet ;Reynolds, James F.


Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
335 KB
Volume
24
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Molecular genetics of Wiedemann-Beckwith
✍ Li, Madeline; Squire, Jeremy A.; Weksberg, Rosanna πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 32 KB πŸ‘ 2 views

Wiedemann-Beckwith syndrome (WBS) is a heterogeneous overgrowth syndrome associated with malformations and an elevated risk of developing embryonal tumors. WBS is a multigenic disorder caused by dysregulation of imprinted growth regulatory genes within the 11p15 region. Elucidation of the genetic ca

Analysis of CDKN1C in Beckwith Wiedemann
✍ Elizabeth Algar; Samantha Brickell; Gillian Deeble; David Amor; Peter Smith πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 359 KB πŸ‘ 1 views
Short Communication. Prenatal detection
✍ B. Fremond; P. Poulain; S. Odent; J. Milon; C. Treguier; J. M. Babut πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 412 KB πŸ‘ 1 views

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

The Beckwith-Wiedemann syndrome phenotyp
✍ Schneid, H.; Vazquez, M.P.; Vacher, C.; Gourmelen, M.; Cabrol, S.; Le Bouc, Y. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 112 KB πŸ‘ 1 views

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