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Rare Genetic Disorder Treatment Hopes for Breakthrough

Hope in a Rare Case: The Fight Against CTNNB1 Syndrome CTNNB1 syndrome is a genetic disorder that affects fewer than 40 children in Canada.

For families like Harper Tanton's, it has been a long and difficult journey searching for answers.

Initially misdiagnosed with cerebral palsy, Harper's parents, Tara and Scott Tanton, refused to accept the diagnosis and dug deeper into medical literature.

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