Research Report

The Omphaloceles: Antenatal Diagnosis and Obstetrical Menagement  

Houssem Ragmoun1 , Abir Agili1 , Abdrahmen Daadoucha2 , Najeh Benhlima3
1 Department of Obstetric Gynecology Ibn El Jazzar Hospital, University hospital assistant in gynecology obstetrics, Ibn El Jazzar street, Kairouan, 3100, Tunisia
2 Department of Radiology Ibn El Jazzar Hospital, University hospital assistant in radiology, Ibn El Jazzar street, Kairouan, 3100, Tunisia
3 Department of Cardiology Ibn El Jazzar Hospital, University hospital assistant in cardiology, Ibn El Jazzar street, Kairouan, 3100, Tunisia
Author    Correspondence author
International Journal of Clinical Case Reports, 2017, Vol. 7, No. 16   doi: 10.5376/ijccr.2017.07.0016
Received: 23 Oct., 2017    Accepted: 27 Nov., 2017    Published: 08 Dec., 2017
© 2017 BioPublisher Publishing Platform
This is an open access article published under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Preferred citation for this article:

Ragmoun H., Ajili A., Daadoucha A., and Benhlima N., 2017, The omphaloceles: antenatal diagnosis and obstetrical menagement, International Journal of Clinical Case Reports, 7(16): 67-72 (doi: 10.5376/ijccr.2017.07.0016)

Abstract

The omphalocele is a rare malformation. Its frequency is estimated to be 1/5000 births. This malformation results from a closing defect of the abdominal wall and it’s frequently associated with other chromosomic abnormalities. We reported three new cases of omphaloceles occurred to 27, 43 and 39 years old patients. The diagnosis by the ultrasound exam was easy and precocious. A fetal karyotype was performed to all the patients and was constantly abnormal. Therefore, the medical termination of the pregnancy was practiced to the three patients. On the occasion of those three observations and a literature review, we remind the diagnostic aspects and the menagement modalities of this congenital malformation.

Keywords
Omphalocele; Parietal defect; Chromosomal aberration; Trisomy 18
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International Journal of Clinical Case Reports
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