Health Research Offers Young Man A Chance to Beat Rare Bone Condition
Discover how a clinical trial at the IU School of Medicine helped Colton overcome a rare genetic bone condition called X-linked hypophosphatemia (XLH).
Bright. Popular. Optimistic. Those are the words Debbie Moore uses to describe her son Colton who, at 16 months of age, was diagnosed with a deforming bone disorder called X-linked hypophosphatemia (XLH). Both uncommon and painful, XLH causes rickets and osteomalacia, or softening of the bones. Patients are typically diagnosed during childhood and have bowed […]
To Read More About Colton, visit the IU School of Medicine Blog: From one generation to the next, research offers a world of opportunity – Blogs