Cantu syndrome is found in countries around the globe. First described in 1982 by J.M. Cantu in several Mexican individuals, it has since been identified in both males and females of various ethnicities worldwide. Although there is currently no specific treatment, recent genetic discoveries offer hope for future breakthroughs in therapy.
Cantu Syndrome Interest Group
Raising awareness and fostering support
Bring hope for potential therapies
Compiling a multinational registry
Our global partnership aims to compile extensive medical and genetic data to explore the genetic links to phenotypical traits in affected individuals.
Offering comprehensive evaluations & support
Providing a setting for clinicians, patients and families to evaluate and research Cantu syndrome's clinical features while fostering social connections.
Offering comprehensive evaluations & support
Providing a setting for clinicians, patients and families to evaluate and research Cantu syndrome's clinical features while fostering social connections.