Open Journal of Pediatrics

Volume 10, Issue 3 (September 2020)

ISSN Print: 2160-8741   ISSN Online: 2160-8776

Google-based Impact Factor: 0.45  Citations  

Oeis Syndrome (Cloacal Exstrophy): About Two Cases Treated at the Mother and Child Teaching Hospital in Cotonou (Benin)

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DOI: 10.4236/ojped.2020.103054    605 Downloads   2,665 Views  Citations

ABSTRACT

Introduction: OEIS syndrome, the most severe form of exstrophy-epispadias complex, is characterized by the existence of an omphalocele, a bladder exstrophy, an anal imperforation and a spina bifida. Case Presentation: Two clinical cases admitted at the first day of life in neonatology department are reported; one was born by caesarean section, weighing 2500 g and the other one vaginally with a weight at 1890 g. The first child’s mother was a primigravid, primiparous and the second mother was multiparous. Prenatal ultrasound was performed in one case. The clinical examination found two exstrophied hemi-bladders with two productive ureteral meatus, separated by a double intestinal orifice, a manifestation of anal imperforation, omphalocele, spina bifida and lumbar vertebral malformations; which corresponds to a typical form of OEIS syndrome. One of the babies had an associated clubfoot. The karyotype could not be performed. Both were dead; the first in the early postoperative period, the second one at 16 days of life without surgery. Conclusion: OEIS syndrome is a rare condition and represents a therapeutic challenge in developing countries. Promoting prenatal diagnosis is essential.

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Gbenou, A. , Assan, B. , Akodjenou, J. , Enianloko, N. , Yasségoungbé, M. and Fiogbe, M. (2020) Oeis Syndrome (Cloacal Exstrophy): About Two Cases Treated at the Mother and Child Teaching Hospital in Cotonou (Benin). Open Journal of Pediatrics, 10, 535-541. doi: 10.4236/ojped.2020.103054.

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