Latest Discovery: “CIROZ” Gene Linked to Heart Defects and Organ Misplacement
Researchers from King Abdullah University of Science and Technology (KAUST) have made a significant breakthrough in understanding the genetic basis of congenital heart defects and abnormal organ placement. The newly identified gene, named “CIROZ,” has been pinpointed as a crucial factor in these medical conditions.
The study, conducted in collaboration with two universities and two hospitals within Saudi Arabia, sheds light on the genetic underpinnings of heritable diseases that are notably prevalent in the region compared to global statistics. This discovery not only advances the scientific community’s understanding of pediatric heart conditions but also opens new avenues for targeted therapies and preventive measures.
Date: February 27, 2025
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