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A toddler is thriving after doctors in the U.S. and Canada used a novel technique to treat her before she was born for a rare genetic disease that caused the deaths of two of her sisters. Ayla Bashir,...
In a medical first, doctors were able to prevent heart and muscle damage using enzyme replacement therapy.
To all outward appearances Ayla Bashir is a normal, happy, 17-month-old child. She began crawling right on time, and today she stands and walks, plays with toys, and has started saying her first words and phrases. The reason she’s able to thrive today is thanks to a new way of treating her rare genetic disease — a form which is often fatal.
A toddler is thriving after doctors in the U.S. and Canada used a novel technique to treat her before she was born for a rare genetic disease that caused the deaths of two of her sisters.
Ayla Bashir, a 16-month-old girl from Ottowa, Canada, is healthy after doctors used a new method to treat her before she was born. She has a rare genetic disease, called Pompe, that killed two of her sisters. But a new treatment seems to be working for Ayla.