Isolated Levocardia with Situs Inversus in a Child: A Rare and Frequently Missed DiagnosisIsolated Levocardia with Situs Inversus – A Rare & Frequently Undiagnosed

Authors

  • Syed Muhammad Azeem Shalamar Medical and Dental College, Lahore, Pakistan. Author
  • Taimoor Saeed Daniyal Shalamar Medical and Dental College, Lahore, Pakistan Author
  • Asad Ramzan Huntsman Cancer Institute, Utah, USA Author
  • Syeda Amna Bashir Rashid Latif Medical and Dental College, Lahore, Pakistan Author
  • Fatima Gilani Shalamar Medical and Dental College, Lahore, Pakistan Author
  • Muhammad Fahad Shahid Shalamar Medical and Dental College, Lahore, Pakistan Author
  • Marryam Anwar Noorda College of Osteopathic Medicine, Provo, Utah, USA Author

DOI:

https://doi.org/10.63075/hgek9509

Abstract

Isolated levocardia with situs inversus (ILSI) is a rare condition in which the heart is located within the left hemithorax with its base-apex axis pointing caudally to the left and with partial or complete inversion of the abdominal viscera. This condition has an estimated incidence of 1 in 22,000 in the general population. This condition is comorbid with various heart defects and is associated with poor prognosis, with only 5-13% of the population surviving more than 5 years.1. Despite high mortality and being associated with congenital forms of severe heart defects, this condition is frequently undiagnosed and is often an accidental finding. In this case report, we describe a 13-year-old girl diagnosed as having complete situs inversus with levocardia, with symptoms only involving the gastrointestinal tract.

Keywords: Phylogenetic Diversity, Ethnobotany, Medicinal Plants, Species Richness, Conservation Biology

 

Downloads

Download data is not yet available.

Downloads

Published

2025-07-22

How to Cite

Isolated Levocardia with Situs Inversus in a Child: A Rare and Frequently Missed DiagnosisIsolated Levocardia with Situs Inversus – A Rare & Frequently Undiagnosed. (2025). Annual Methodological Archive Research Review, 3(7), 427-431. https://doi.org/10.63075/hgek9509