Results 21 to 30 of about 550 (151)

Pentalogy of Cantrell: the complete spectrum. [PDF]

BMJ Case Rep, 2014
A healthy 25-year-old primigravida, without a history of teratogenic exposition, presented to our hospital with a first trimester routine ultrasonographic examination showing two major fetal defects: gastrosquisis (figure 1 and video 1) and ectopia cordis (video 2).
Martins CF, Serras I, Santos AV, Costa Braga A.   +3 more
europepmc   +5 more sources

Coincidence of Incomplete Pentalogy of Cantrell and Meningomyelocele in a Dizygotic Twin Pregnancy [PDF]

Case Reports in Obstetrics and Gynecology, 2015
Pentalogy of Cantrell is an extremely rare and lethal syndrome. Ectopia cordis is frequently found in fetuses with POC but not required for incomplete forms. Likewise, meningomyelocele is a relatively uncommon neural tube defect affecting central nervous
Hakan Timur, Aytekin Tokmak, Hatice Bayram, Esra Şükran Çakar, Nuri Danışman   +4 more
doaj   +2 more sources

Pentalogy of Cantrell: Comprehensive Multimodal Imaging Evaluation in an Adult With Ectopia Cordis. [PDF]

JACC Case Rep
Alanís-Naranjo JM, De la Cruz-Pelayo J, de la Mora-Cervantes R, Gamboa-Abundis OA, Meave-González A, Cruz-Marmolejo MÁ.   +5 more
europepmc   +3 more sources

Pentalogy of Cantrell: A case report

Journal of Research in Medical Sciences, 2011
Cantrell′s pentalogy (CP), a rare congenital malformation, consists of the supraumbilical abdominal wall defect, the sterna lower part defect and agenesis of the anterior portion of the diaphragm, an absence of the diaphragmatic part of the pericardium ...
Amir Hossein Jafarian, Abbas Ali Omidi, Alireza Fazel, Hamed Sadeghian, Bahareh Joushan   +4 more
doaj   +2 more sources

Pentalogy of Cantrell. A stillbirth case report

Case Reports, 2022
Introduction: Pentalogy of Cantrell is a rare congenital disorder characterized by midline birth anomalies. Its embryological origins are related to anomalies of the abdominal wall that prevent the closure of the thorax.
Maribel Palencia Palacios, Blanca Viviana Fajardo Idrobo, Valentina López Mosquera, Jaime Antonio Álvarez Soler   +3 more
doaj   +1 more source

Pentalogy of Cantrell

Donald School Journal of Ultrasound in Obstetrics and Gynecology, 2012
[No abstract available ...
Mohmmed S.D.E., Elrayah N., Noor H., Ahmed B.   +3 more
openaire   +5 more sources

Pentalogy of Cantrell: A case report of probable pentalogy of Cantrell in a full-term neonate [PDF]

Iranian Journal of Neonatology, 2021
Background: Pentalogy of Cantrell (PC) is an extremely rare congenital anomaly which was first described in 1985. The incidence of the PC has been reported to vary from 5.5-7.9 cases per million live births.
Mina Khosravifar, Homa Babaei, Nona Rahbari   +2 more
doaj   +1 more source

Amniotic band syndrome and limb body wall complex in Europe 1980–2019

American Journal of Medical Genetics Part A, Volume 191, Issue 4, Page 995-1006, April 2023., 2023
Abstract Amniotic band syndrome (ABS) and limb body wall complex (LBWC) have an overlapping phenotype of multiple congenital anomalies and their etiology is unknown. We aimed to determine the prevalence of ABS and LBWC in Europe from 1980 to 2019 and to describe the spectrum of congenital anomalies.
Jorieke E. H. Bergman, Ingeborg Barišić, Marie‐Claude Addor, Paula Braz, Clara Cavero‐Carbonell, Elizabeth S. Draper, Luis J. Echevarría‐González‐de‐Garibay, Miriam Gatt, Martin Haeusler, Babak Khoshnood, Kari Klungsøyr, Jennifer J. Kurinczuk, Anna Latos‐Bielenska, Karen Luyt, Danielle Martin, Carmel Mullaney, Vera Nelen, Amanda J. Neville, Mary T. O'Mahony, Isabelle Perthus, Anna Pierini, Hanitra Randrianaivo, Judith Rankin, Anke Rissmann, Florence Rouget, Gerardine Sayers, Bruno Schaub, Sarah Stevens, David Tucker, Christine Verellen‐Dumoulin, Awi Wiesel, Erica H. Gerkes, Annie Perraud, Maria A. Loane, Diana Wellesley, Hermien E. K. de Walle   +35 more
wiley   +1 more source

Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcome

Prenatal Diagnosis, Volume 43, Issue 2, Page 183-191, February 2023., 2023
Abstract Objective Omphalocele is known to be associated with genetic anomalies like trisomy 13, 18 and Beckwith–Wiedemann syndrome, but not with Turner syndrome (TS). Our aim was to assess the incidence of omphalocele in fetuses with TS, the phenotype of this association with other anomalies, their karyotype, and the fetal outcomes.
Ivonne Bedei, Karl‐Philipp Gloning, Luc Joyeux, Matthias Meyer‐Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai‐Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M. Jahns, Annegret Geipel, Ismail Tekesin, Michael Elsässer, Lucas Wilhelm, Ingo Gottschalk, Jan‐Erik Baumüller, Cahit Birdir, Andreas Schröer, Felix Zöllner, Aline Wolter, Johanna Schenk, Tascha Gehrke, Alicia Spaeth, Roland Axt‐Fliedner   +25 more
wiley   +1 more source

First reported case of Pentalogy of Cantrell variant with good outcome in a 32 week gestational age monozygotic twin with twin-twin transfusion syndrome

Journal of Pediatric Surgery Case Reports, 2019
We report a case of a 32 week gestational age preterm monozygotic twin neonate with a rare variant of Pentalogy of Cantrell who presented with severe respiratory distress syndrome, possible pulmonary hypoplasia, large congenital diaphragmatic hernia ...
Preethi Srinivasakumar, Ganapathy Rama, Nathan Jesse, Rogers G. Howell, Joseph Lawrence Brady, Jr., Tania Tejera Morales, Hima Maramreddy, Jenna Hogan, Graham H. Cosper, Thomas Schmelzer, Daniel A. Bambini, Andrew Schulman, Jay Kothadia   +12 more
doaj   +1 more source