For patients recovering from strokes, injuries, limb loss, and more, Zale Lipshy Pavilion offers inpatient rehabilitation programs from a team of experts.
Using an advanced gene editing technology called CRISPR, our team of scientists at UT Southwestern has been able to stop the progression of Duchenne muscular dystrophy in animals and human cells – a breakthrough that could ultimately change the prognosis for the most common fatal genetic disease in boys.
Sarah initially was admitted at Children’s Health and we were consulted when it was discovered that she had acute flaccid myelitis, a rare type of transverse myelitis thought to be triggered by a viral infection. We’re one of only two dedicated transverse myelitis centers in the world, and we’re the only one with a multidisciplinary focus on children.
