Related Experiment Video
Updated: Jan 16, 2026

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform
Published on: August 17, 2022
From screening to strategy: Clinical implications of COL4A3/COL4A4 variants found in reproductive genetic testing
Gráinne Butler1,2,3, David J Amor4,5,6, Catherine Quinlan4,5,6
1Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia. grainne.butler@rch.org.au.
Abstract:
Reproductive genetic carrier screening (RGCS) is expanding in both public and private healthcare. The primary aim is to identify carrier status for genetic disorders, inform reproductive decision making and promote reproductive autonomy. As screening panels have increased, the potential for findings with personal health implications rises. We report the prevalence of COL4A3/COL4A4 heterozygous variants within a population undergoing RGCS in a private setting and propose a comprehensive management plan for the ongoing care of this patient cohort. Acknowledging that comprehensive guidelines exist for genetic testing and management of Alport syndrome as a broad patient group, this communication seeks to highlight the increasingly common finding of autosomal dominant Alport syndrome and proposes accessible and practical strategies for the clinicians encountering these patients.

