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New research into genetic links to stuttering tipped to be 'life-changing' for those with speech condition

New research into genetic links to stuttering tipped to be 'life-changing' for those with speech condition

For 10-year-old Harriet Hewitt, talking in front of people used to be a challenge.
Growing up with a stutter, it was difficult to find her voice.
"I couldn't really say sentences that I wanted," she said.
"I would basically just want to be like other kids, but I don't want to be like them anymore."
Now she speaks with confidence, after mostly overcoming her stutter — a condition which has affected four generations of her family.
Stuttering affects more than 400 million people worldwide, and most commonly emerges in early childhood around the ages of two to four.
Half of Harriet's siblings have stutters, along with her mum, grandmother, grandfather, great-grandfather and other family members.
Now a new global study has identified a hereditary link associated with stuttering.
Harriet and her family gave DNA samples, some of the 1,380 that came from WA, as a part of a global study that has discovered stutterers have a hereditary link.
The research was conducted by the Curtin Stuttering Treatment Clinic in collaboration with Wayne State University in Detroit.
It involved samples from one million people and identified 48 genes associated with the condition, paving the way for clinicians to predict which family members will experience the condition.
Research co-author and Curtin Stuttering Treatment Clinic founder, Professor Janet Beilby said the findings were groundbreaking.
"We found consistent DNA results, 48 of them, and in addition to that we found 57 [genomic] hot spots so it's very exciting because with these hot spots we can dig further," Professor Beilby said.
Professor Beilby said the findings will enable clinicians to intervene earlier, crucial in treating the speech disorder.
"Based on what we've found in this research, we will be able to take a DNA sample and predict if the individual is likely to stutter or not," Professor Beilby said.
"It means those particular young people will be offered early intervention straight away hopefully, and in doing that we can curtail what can be otherwise a lifelong disability.
Associate Professor Beilby said the research would be "life-changing for all those children who stutter".
"Most children with a speech or language disorder will be bullied at school and adults who stutter may face challenges in the workplace that can negatively affect their mental health and social wellbeing,' she said.
Harriet's mum Simone Hewitt said she is hopeful the next generation of her family will reap the benefits of the study.
"When I look at my whole family you always wonder if there is a genetic link and what I think is absolutely amazing is that we now know there is a genetic component," Ms Hewitt said.
"For my family I think it's very exciting, I think about what it could do for my grandchildren because obviously we have a strong link with stuttering and communication," Ms Hewitt said.
"I think it would be absolutely amazing to know my grandchildren as infants can be tested and go right, we can start now."
Harriet said she is happy the research will have positive effects on others.
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