This website provides information on patients with mutations in the Fibronectin 1 (FN1) gene, including clinical data, molecular data, management and research options.

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the FN1 gene.
Choose page:
•    Glomerulopathy with fibronectin deposits type 2
•    FN1-related Spondylometaphyseal dysplasia, corner fracture type

Clinicals who identify a patient with a mutation in FN1 are invited to submit clinical and molecular information to the database.

Jade England, MD, MSc, University of Montreal, Montreal, Canada, jade.england@umontreal.ca

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

Philippe Campeau, MD, Principal Investigator, CHU Sainte Justine, Mother and Child University Hospital, Montreal, Canada, p.campeau@umontreal.ca

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