Case report: Heterotaxy syndrome with polysplenia

المؤلفون

  • Salem Abdullah Asselhab, Emhmed Mohamed Saaid

الملخص

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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التنزيلات

منشور

2018-12-20

إصدار

القسم

المقالات