20 Years of Research and Progress — A Story of Collaboration
By WORLDSymposia on February 09, 2024
This is the story of a WORLDSymposium collaboration that began with a Canadian physician's call to a Duke colleague, seeking help for a family who had already lost children to Pompe disease. Duke colleagues, informed by UCSF's intrauterine therapy approach, initiated the collaboration at... Fetal therapy offers hope for fetus diagnosed with Hunter Syndrome
By Molly McCrea and Juliette Goodrich on January 23, 2024
Some parents-to-be have to face the terrifying news that their unborn child has been diagnosed with a life-threatening genetic disorder. But thanks to a medical team at a Bay Area hospital, there is amazing new hope in a fetal therapy that may spare their unborn child serious outcomes. The Surgeon Set on Curing Genetic Diseases Before Birth
By Kirsten Weir on June 23, 2023
UCSF’s Tippi MacKenzie is leading groundbreaking clinical trials of therapies aimed at stopping fetuses from developing devastating disorders. Five-year-old Elianna loves running around with her big brother in their yard on the Hawaiian island of Kauai. She isn’t afraid to get dirty, is learning to... After Losing 2 Children to Rare Genetic Disease, Family Celebrates Healthy Daughter
By Garvin Thomas on November 17, 2022
By the time 2021 came around, Sobia Qureshi and Zahid Brashir were well aware of the odds. For better and worse, they had lived them.
The Ottowa, Canada, couple had given birth to four children. Two of them, a son and a daughter, are healthy. Two others, both daughters, died before the age of two... The Disease Took Zara, Then Sara. Could Ayla Be Saved?
By Gina Kolata on November 09, 2022
Two sisters in one family died from a genetic disorder. Before a third child with the disease was born, doctors hatched a plan to spare her of its effects. For the first time, doctors have successfully treated a fetus by infusing a crucial enzyme into its minuscule umbilical cord, halting an... Fetal Therapy Offers Hope for Patients
By Jess Berthold on November 09, 2022
When Zahid and Sobia Bashir discovered their fetus had the same genetic disease that took the lives of two of their young children, they didn’t hesitate to sign up for a promising but experimental new therapy. “I found out (the therapy) was a possibility and I was kind of in shock; I couldn’t...