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Complete and Incomplete Pentalogy of Cantrell [PDF]

open access: yesChildren, 2019
Pentalogy of Cantrell (PC) is a malformation characterized by defects in the ventral abdominal wall, lower sternum, diaphragmatic pericardium, anterior diaphragm associated with omphalocele, thoraco-abdominal ectopia cordis, diaphragmatic hernia, and ...
Ranjit I Kylat
exaly   +7 more sources

Pentalogy of Cantrell Associated with Ectopia Cordis: A Case Report [PDF]

open access: yesPediatric Health, Medicine and Therapeutics, 2022
Muneer Fazea,1,2 Mansour Alhameli,2,3 Faisal Ahmed,4 Mohammad Reza Askarpour,5 Wafa Murshed,2 Azizh Jarwsh,2 Amal Alkbous2 1Department of Radiology, School of Medicine, Ibb University of Medical Sciences, Ibb, Yemen; 2Department of Radiology, Al-Ma’amon ...
Mohammad Reza Askarpour   +2 more
exaly   +4 more sources

Pentalogy of Cantrell [PDF]

open access: yesSeminars in Pediatric Surgery, 2019
Pentalogy of Cantrell is a constellation of five congenital defects that pose a unique challenge for surgeons. Defects of the heart, pericardium, diaphragm, sternum, and anterior abdominal wall are pathognomonic. Although the incidence is low, it is critical to identify it in a timely fashion in order to adequately address all aspects. Early diagnosis,
Raoud Marayati   +2 more
exaly   +5 more sources

Pentalogy of Cantrell: a case report [PDF]

open access: yesBJR|case reports, 2015
Pentalogy of Cantrell is a rare condition comprising anterior diaphragmatic defect, ventral abdominal wall defect, pericardial defect, intracardiac anomalies and lower sternal defect. Both sporadic and genetic causes are proposed.
A R Patil, L S Praveen, V Ambica
doaj   +5 more sources

Pulsating abdominal mass in a newborn – Pentalogy of Cantrell with left ventricular diverticulum [PDF]

open access: yesAnnals of Pediatric Cardiology, 2023
Pentalogy of Cantrell is a rare congenital anomaly involving the anterior diaphragm, pericardium, sternum, peritoneum, and associated intracardiac defects.
Nabeel Faisal   +5 more
doaj   +2 more sources

Clinical and ultrasound findings of pentalogy of Cantrell in a newborn: A case report [PDF]

open access: yesFrontiers in Pediatrics, 2022
BackgroundPentalogy of Cantrell is a rare and deadly syndrome, manifesting as intracardiac anomalies and ventricular diverticulum. Echocardiographers have an insufficient understanding of pentalogy of Cantrell, which may lead to missed diagnoses ...
Dan Wang   +5 more
doaj   +2 more sources

Pentalogy of Cantrell in Two Neonate Littermate Puppies: A Spontaneous Animal Model Suggesting Familial Inheritance [PDF]

open access: yesAnimals, 2023
Developmental anomalies are an important cause of stillbirth and early perinatal death in companion animals. Many of these disorders remain poorly understood and provide an opportunity as a spontaneous animal model for human disease.
Wilson So   +3 more
doaj   +2 more sources

Radiological findings of partial expression pentalogy of Cantrell and other multiple congenital anomalies: A rare case report [PDF]

open access: yesRadiology Case Reports, 2022
Pentalogy of Cantrell is a rare syndrome of anomalous malformation. In the present case, the syndrome was initially diagnosed as a complete pentad, including a supra-umbilical abdominal wall defect, a sternal defect, pericardial defects, an anterior ...
Ratih Sulistyowati, MD   +1 more
doaj   +2 more sources

Pentalogy of Cantrell: Is Echocardiography Sufficient in the Neonatal Period? [PDF]

open access: yesEuropean Journal of Pediatric Surgery Reports, 2017
Pentalogy of Cantrell is a rare syndrome that is characterized by varying degrees of midline wall defects and congenital cardiac anomalies. A left ventricular diverticulum (LVD) is defined as partial ectopia cordis, can be part of the pentalogy of ...
Elke Zani-Ruttenstock   +3 more
doaj   +2 more sources

Pentalogy of cantrell: Reconstructive challenges of two complete cases in a resource-constrained setting [PDF]

open access: yesJournal of Indian Association of Pediatric Surgeons, 2021
Pentalogy of Cantrell (POC) is a very rare congenital anomaly and treatment has remained a challenge worldwide owing to extensive reconstructive surgeries, more so in resource-constrained settings. We, therefore, report two cases of complete POC.
Jideofor Okechukwu Ugwu   +6 more
doaj   +2 more sources

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