𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Prenatal sonographic diagnosis of beckwith-wiedemann syndrome in association with a single umbilical artery

✍ Scribed by Hiromi Hamada; Yutaka Fujiki; Mana Obata-Yasuoka; Hideki Watanabe; Naoki Yamada; Takeshi Kubo


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
463 KB
Volume
29
Category
Article
ISSN
0091-2751

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Beckwith‐Wiedemann syndrome is an inherited disorder most commonly characterized by prenatal or postnatal overgrowth, macroglossia, omphalocele, unusual earlobe creases, and increased risk of neoplasia. Several reported cases of this syndrome have been prenatally diagnosed, but no report has described the occurrence of this syndrome in association with a single umbilical artery. We report a case in which prenatal sonographic examination demonstrated fetal overgrowth, macroglossia, and omphalocele together with a single umbilical artery; our prenatal diagnosis of Beckwith‐Wiedemann syndrome was confirmed after birth of the infant. The possibility of this syndrome should be considered when performing a detailed sonographic examination of a fetus with a single umbilical artery. Β© 2001 John Wiley & Sons, Inc. J Clin Ultrasound 29:535–538, 2001.


πŸ“œ SIMILAR VOLUMES


Prenatal sonographic diagnosis of laryng
✍ Israel Meizner; Israelit Sherizly; Reuven Mashiach; Joseph Shalev; Dvora Kedron; πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 514 KB

Congenital laryngeal atresia is an extremely rare anomaly that in most cases is incompatible with life. About 50% of cases involve other major malformations. Prenatal sonographic diagnosis of this condition has been described only 6 times. We present a case in which prenatal sonographic examination

Prenatal diagnosis of monosomy 10q25 ass
✍ Yi-Pei Chung; Hsiao-Lin Hwa; Li-Hui Tseng; Ming-Kwang Shyu; Chien-Nan Lee; Jin-C πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 109 KB πŸ‘ 1 views

The association of rare chromosomal rearrangements involving a specific 10q breakpoint with a single umbilical artery (SUA) and sex reversal has never been reported. This report describes the case of a fetus with prenatal ultrasound features of severe intrauterine growth retardation (IUGR), congenit

Prenatal sonographic diagnosis of short
✍ David M. Sherer; Mudar Dalloul; Olusegun Ajayi; Mila Kheyman; Margarita Sokolovs πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 126 KB

## Abstract Short umbilical cords are associated with fetal anomalies, often including those with decreased or absent fetal movement, fetal akinesia/hypokinesia sequence, and restrictive dermopathies and aneuploidy. In normal fetuses, abnormally short umbilical cords have been associated with an in

PRENATAL DIAGNOSIS OF PARTIAL MONOSOMY 3
✍ CHIH-PING CHEN; FEN-FEN LIU; SHEAU-WEN JAN; SHUAN-PEI LIN; CHUNG-CHI LAN πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 737 KB

The prenatal and postnatal findings of a fetus with partial deletion of 3p25+pter and duplication of 2p25.3-ipter are described. The proband postnatally displayed mental and growth retardation, psychomotor delay, microcephaly, ptosis, micrognathia, a narrow palate, and cryptorchidism. All of these a

Prenatal diagnosis of de novo interstiti
✍ Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; Chun-Yu Chuang πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 144 KB πŸ‘ 3 views

De novo interstitial 16q deletion diagnosed in utero has not previously been reported. We present a case of fetal de novo interstitial 16q deletion associated with the sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones. Genetic amniocentesis