Title of article :
Prenatal Diagnosis of an Unusual Phenotype of Cantrell’s Pentalogy: Case Report, and Literature Review
Author/Authors :
Aivasovsky-Trotta ، Ivan Faculty of Medicine - University of La Sabana , Vergara-Cardenas ، Sergio Faculty of Medicine - University of La Sabana , Ferrer-Marcano ، Amenaida Faculty of Medicine - University of La Sabana , Rincones-Rojas ، Lorena Faculty of Medicine - University of La Sabana , Prieto-Soler ، Carolina Faculty of Medicine - University of La Sabana , Bracho-Fernández ، Ana Medical Genetics Unit - Metropolitan Polyclinic , Fernández-González ، Isabel Medical Genetics Unit - Metropolitan Polyclinic , Celis ، Luis Gustavo Faculty of Medicine - University of La Sabana
From page :
85
To page :
91
Abstract :
Background: Cantrell’s pentalogy (CP) is a rare congenital disease caused by morphological changes in the mesoderm. Defects of the lower sternum with ectopia cordis, midline supraumbilical abdominal wall, anterior diaphragm, diaphragmatic pericardium, and cardiac alterations are the related symptoms.Case report: The case report is a newborn boy with a prenatal diagnosis of abdominal wall defect caused by pentalogy of Cantrell class 1 and initial measures were taken to prevent adverse outcomes.  Congenital syndromic disease, such as CP, is likely to be treated with early prevention and adequate prenatal controls. Also, early diagnosis facilitates effective clinical and surgical management and thus leads to a positive prognosis.Conclusion: Finally, it has been established that proper decisionmaking about therapeutic possibilities during the early years may improve the quality of life and longevity in this population.
Keywords :
Congenital abnormalities , Ectopia cordis , Heart diseases , Hernia , Infant , Newborn , Pentalogy of cantrell , Umbilical
Journal title :
Iranian Journal of Neonatology (IJN)
Journal title :
Iranian Journal of Neonatology (IJN)
Record number :
2684274
Link To Document :
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