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Creating a New, Hopeful Future at UTMB

The institution's gene therapy work gives children like Knova a chance at a life that, until recently, wasn’t possible.
Baby holding a green stuffed toy while seated indoors near colorful toys.

Racing against rare SMA diagnosis, UTMB gene therapy team gave newborn a chance

Spinal muscular atrophy (SMA) is a rare inherited neuromuscular condition that causes muscles throughout the body to weaken. It happens because a specific gene, called SMN1, is missing or is not working correctly.

UTMB Health designated as first Qualified Treatment Center in Texas for Zevaskyn

UTMB Health becomes a national leader in treating ultra-rare skin disease RDEB, earning designation as a Qualified Treatment Center for an FDA-approved gene therapy bringing first-of-its-kind care closer to home.
An adult and a toddler sit together on the floor of a living room, looking at an open picture book, with a couch and houseplant visible in the background

Houston Moms + UTMB Geneticist Dr. Erin Cooney talk about new treatments that are changing the future of patients with genetic conditions

Parents shouldn’t have to navigate genetic conditions alone. In this month’s Houston Moms + UTMB Health video, Dr. Erin Cooney explains how her team walks alongside families — helping them find clarity, treatment options, and support for the future.
Young child seated in a padded clinic chair, holding a teddy bear, wearing a blue shirt and colorful socks, inside a medical room with soft lighting and patterned furniture

A Life-Changing Day for Max: Hope Through Gene Therapy

At UTMB Health, every day brings new possibilities for patients like Max—a young man living with Duchenne muscular dystrophy.

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