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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 ....

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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. ....

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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. ....

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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 ....

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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 ....

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