Case report: Heterotaxy syndrome with polysplenia

Authors

  • Salem Abdullah Asselhab, Emhmed Mohamed Saaid

Abstract

Heterotaxy syndrome is a rare complex syndrome characterized by cardiac and extra cardiac congenital malformations. The syndrome is divided into two main groups; right isomerism (Ivemark syndrome, asplenia) and left isomerism (polysplenia syndrome). We report a polysplenia syndrome with agenesis of head and uncinate process of the pancreas in a 30-year-old woman who was admitted to our clinic with complaints of loin pain and dysuria. 

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Published

2018-12-20

How to Cite

Salem Abdullah Asselhab, Emhmed Mohamed Saaid. (2018). Case report: Heterotaxy syndrome with polysplenia. Journal of Medical Sciences, 13(1). Retrieved from https://sebhau.edu.ly/journal/index.php/joms/article/view/322

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Articles