This website provides information on patients with mutations in the GINS complex subunit 3 (GINS3) gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the GINS3 gene is a multisystem disorder called Meier-Gorlin-like syndrome (MG-like) syndrome characterized by microtia, patellar hypoplasia, and short stature.

Not all individuals with a mutation in the GINS3 gene have these features.

This website was created to share and collect information about clinical, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the GINS3 gene.

Philippe Campeau, MD, CHU Sainte-Justine Research Center, University of Montreal, Montreal, Canada, p.campeau@umontreal.ca

Coralie Michaud, MD, University of Montreal, Montreal, Canada, coralie.michaud@umontreal.ca