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Minnesota family fighting for daughter with ultra-rare genetic mutation, others like herWhen she was 1.5 years old, Mae was diagnosed with the neuro-developmental disorder, CTNNB1 Syndrome. "She's non-verbal, she's unable to walk unassisted," said Emily Knopik, Mae's mother.
Matilda Monerawela, aged 10, was born with a neurodevelopmental disorder caused by mutations in the CTNNB1 gene, which plays a vital role in providing instructions for making a protein involved in ...
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