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Abdominal wall defects: omphalocele

Alteraciones de la pared abdominal: onfalocele




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Reflection Articles

How to Cite
Tinoco Guzmán, N. J. ., Ocampo Padilla, P. ., Galindo Angarita, K. J. ., Argüello Arciniegas, L. D., Alonso Cardenas, D. M. ., Duarte Tayo, C. D. ., Tinoco Serrano, D. L. ., Castro Guerrero, F. J. ., Garzón Palacios, L. M. ., Sandoval Bastidas, M. C. ., Rendón Carrero, M. V. ., Solarte Moncayo, S. I. ., & Suárez Camacho, A. . (2021). Abdominal wall defects: omphalocele. Journal of Medicine and Surgery Repertoire, 33(1), 105-111. https://doi.org/10.31260/RepertMedCir.01217372.1288

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Nestor Julian Tinoco Guzmán

    Patricia Ocampo Padilla
      Karen Johana Galindo Angarita
        Laura Daniela Argüello Arciniegas
          Deassy Mayerly Alonso Cardenas
            Carol Dayanna Duarte Tayo
              Doris Lorena Tinoco Serrano

                Fanny Jineth Castro Guerrero
                  Lina María Garzón Palacios
                    María Camila Sandoval Bastidas

                      María Verónica Rendón Carrero
                        Sergio Iván Solarte Moncayo

                          Alfonso Suárez Camacho

                            Nestor Julian Tinoco Guzmán,

                            Esp. Cirugía Pediátrica, Instructor Asistente Fundación Universitaria de Ciencias de la Salud. Bogotá DC, Colombia.


                            Patricia Ocampo Padilla,

                            Esp. Cirugía Pediátrica, Instructor Asistente Fundación Universitaria de Ciencias de la Salud. Bogotá DC, Colombia.


                            Karen Johana Galindo Angarita,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.


                            Laura Daniela Argüello Arciniegas,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.


                            Deassy Mayerly Alonso Cardenas,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.


                            Carol Dayanna Duarte Tayo,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.


                            Doris Lorena Tinoco Serrano,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.


                            Fanny Jineth Castro Guerrero,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.


                            Lina María Garzón Palacios,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.


                            María Camila Sandoval Bastidas,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia.


                            María Verónica Rendón Carrero,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia


                            Sergio Iván Solarte Moncayo,

                            Facultad de Medicina, Fundación Universitaria de Ciencias de la Salud, Bogotá DC, Colombia


                            Alfonso Suárez Camacho,

                            Esp. en Anatomía, fisiología y genética. Fundación Universitaria de Ciencias de la Salud. Bogotá DC, Colombia.


                            Introduction: abdominal wall defects are congenital malformations associated with herniated abdominal organs, such as omphalocele. Its estimated prevalence is 1 per 10.000 live births in western countries. In Colombia the prevalence of omphalocele remains unknown. Omphalocele may be pre or postnatally diagnosed. A series of systemic clinical exams, secondary diagnostic evaluation and assessment for accompanying anomalies, are necessary. Treatment has improved survival rate to 70 and 95%. Objective: to increase awareness of this anomaly and correlate genetic, environmental and clinical findings and complementary exams to enable the early diagnosis and referral of these patients to receive optimal treatment which will reduce mortality. Materials and methods: updated literature review using Pubmed, UpToDate and ClinicalKey search engines, focused on systematic reviews, clinical cases and main international clinical practice guidelines. Found data was submitted to the head of the pediatric surgery department and to the publications division for their information, review and approval Results: 17 articles published in the last 5 years including the most relevant which contained current clinical evidence, were selected. Discussion and conclusions: recent studies have evidenced new findings that have improved survival and reduced mortality in the last 50 years.


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