Case report: Heterotaxy syndrome with polysplenia

المؤلفون

  • Salem Abdullah Asselhab, Emhmed Mohamed Saaid

DOI:

https://doi.org/10.51984/joms.v13i1.322

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. 

التنزيلات

تنزيل البيانات ليس متاحًا بعد.

التنزيلات

منشور

2018-12-20

إصدار

القسم

المقالات

كيفية الاقتباس

Case report: Heterotaxy syndrome with polysplenia. (2018). مجلة العلوم الطبية, 13(1). https://doi.org/10.51984/joms.v13i1.322