amniotic band syndrome
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2022 ◽  
Vol 19 (4) ◽  
Author(s):  
K S Kumaravel ◽  
R Sujetha ◽  
T Palanivelraja ◽  
S Gobinathan ◽  
P Sampathkumar

Author(s):  
Osamu Yazawa ◽  
Daisuke Hirokawa ◽  
Kaede Okamoto ◽  
Mio Tanaka ◽  
Jun Shibasaki ◽  
...  

Author(s):  
Mekonen Eshete ◽  
Muhidin Abdo Banko ◽  
Abiye Hailu ◽  
Abeje Brhanu ◽  
Peter Mossey ◽  
...  

AbstractAmniotic band syndrome (ABS) is not a commonly seen birth defect; however, it may have the potential to be severe and life-threatening requiring adequate attention. We present a severe case of amniotic band syndrome which encircled the head of the neonate tightly causing severe deformity. In this case report, the amniotic band encircled the head causing a severe bilateral Tessier 7 cleft. To our knowledge, this is the most severe type of ABS reported in the literature thus far.Level of evidence: Level V, risk / therapeutic study.


2021 ◽  
Vol 43 (2) ◽  
pp. 120
Author(s):  
R. C. Fernandopulle ◽  
R. Sathanandarajah ◽  
W. M. C. L. Gunarathna

Author(s):  
Aissatou Mbodji ◽  
Mouhamadou Wade ◽  
Mamour Gueye ◽  
Mame D. Ndiaye ◽  
Aliou D. Dia ◽  
...  

Amniotic band syndrome is a pathology affecting the extremities of the fetus. It is uncommon with rates around 1 per 10,000 births. The pathophysiology is poorly understood until now with several theories reported in the literature. The diagnosis is most often made at birth. We reported a case of a 40 year old patient with no particular history who had consulted for spontaneous premature rupture of membranes in a 20 weeks pregnancy. The diagnostic of amniotic band syndrome was made after the delivery with amputation of a limb, amniotic syndactilia and deformation of the right foot in equinovarus.


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Mizuki Nakashima ◽  
Takashi Iizuka ◽  
Kyosuke Kagami ◽  
Rena Yamazaki ◽  
Masanori Ono ◽  
...  

Abstract Background Amniotic band syndrome is a rare phenomenon, but it can result in serious complications. We report herein our experience of amniotic band syndrome in a monochorionic diamniotic twin pregnancy where rupture of the dividing membrane occurred early in the second trimester. Case Presentation A 29-year-old nulliparous woman was referred to us for management of her monochorionic diamniotic twin pregnancy at 10 weeks of gestation. When we were unable to identify a dividing membrane at 15 weeks of gestation using two-dimensional ultrasonography, we used three-dimensional ultrasonography to confirm its absence. Both modalities showed that the left arm of baby B was swollen and attached to a membranous structure originating from the placenta at 18 weeks of gestation. Tangled umbilical cords were noted on magnetic resonance imaging at 18 weeks of gestation. Emergency cesarean delivery was performed at 30 weeks of gestation because of the nonreassuring fetal status of baby A. The left arm of baby B had a constrictive ring with a skin defect. Both neonates had an uncomplicated postnatal course and were discharged around 2 months after delivery. Conclusions Attention should be paid to the potential for amniotic band syndrome if rupture of the dividing membrane between twins is noted during early gestation.


2021 ◽  
Vol 15 (5) ◽  
pp. 220-224
Author(s):  
Chris Barber

The purpose of this series is to highlight a range of rare health conditions. Rare health conditions are those that affect no more and usually fewer than 1 person in every 2000 and many HCAs and nurses will encounter some of these conditions, given the high number of them. This 47th article will explore two of these conditions, Gorham's disease and amniotic band syndrome, and offer a focus on the ‘strengths-based model’ of healthcare assessment and planning.


2021 ◽  
Vol 41 (5) ◽  
pp. 301-305
Author(s):  
Melissa Esparza ◽  
Elaine Tran ◽  
Benjamin Stephens Richards ◽  
Chan-hee Jo ◽  
Claire Shivers ◽  
...  

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