Mila's legacy: The little girl who could change how medicines are made in Britain
Mila Vitarello was just 10 when she died from Batten’s disease. Now, the fight to find a cure for rare genetic disorders arrives in Britain
Source: telegraph.co.uk
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A Somerville boy has one of world's rarest diseases
The parents of 19-month-old Lucas Guo hope to raise $10 million to find a cure or treatment for ZTTK syndrome, a complex neurological disorder caused by a genetic mutation.
Source: bostonglobe.com
An untreatable disease devastated a 4-year-old boy—until a Boston doctor stepped in
Alternating Hemiplegia of Childhood, or AHC, could see a new treatment thanks to a team of neurologists at Boston Children's Hospital.
Source: wgbh.org
Google DeepMind's AI tool could pinpoint our genetic faults
There’s been plenty of worrying about the damage AI could do, but discoveries like the Google tool that can pluck harmful genome mutations from thousands of minute-but-benign ones show how AI can accelerate progress on the most vexing questions about human biology and health
Source: moneycontrol.com
Parents crack the genetic code of their child's condition to find personalised treatment
When Niamh McDonagh was born with an extremely rare genetic variation, her parents were told little could be done for her. They decided to use their skills as biologists to recreate the specific mutation and understand it better. Their work is based on cutting-edge research helping to develop targeted medicines
Source: irishexaminer.com