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Updated: Jul 5, 2026

Cox-Maze IV Procedure Concomitant with Valvular Surgery In Situs Inversus Dextrocardia: A Single-Center Experience in China
Published on: February 11, 2022
Klippel-Feil syndrome with situs inversus--a rare association
Jawad Jalil1, Mobeen Shafique, Nasser Rashid Dar
1Department of Paediatrics, Combined Military Hospital, Bahawalpur. jawadjalil2002@hotmail.com
Abstract:
Klippel-Feil Syndrome (KFS) is a congenital anomaly characterized by a defect in the formation or segmentation of the cervical vertebrae. The clinical triad consists of short neck, low posterior hairline and limited neck movement. Multiple congenital anomalies have been associated with this disease. This is a case of KFS in a young girl along with situs inversus, which is an extremely rare association. Various systemic associations occurring in this multi-system disorder are also discussed.
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