How APOL1 gene mutations in ACB communities increase their risk of kidney disease

This presentation discusses one of the genetic factors that causes disparities in kidney health in ACB communities. The discussion surrounds a mutation in the APOL1 gene, found in many individuals in ACB communities, particularly those with West African ancestry. The presentation includes underlying causes, diagnosis, and treatment of black patients with kidney disease who may have this gene mutation.

Speaker – Kayla-Rae Barnes

Kayla-Rae Barnes is a second-year Health Sciences student at Queen’s University. She is passionate about promoting health equity and education in marginalized communities. As an aspiring healthcare professional, she is dedicated to making a positive impact in the healthcare industry. 

Q & A