Case report: Heterotaxy syndrome with polysplenia
DOI:
https://doi.org/10.51984/joms.v13i1.322Keywords:
Heterotaxy syndrome,, Polysplenia syndrome,, Pancreatic agenesis,, Congenital malformations,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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