In the debut episode, Elva teams up with singer-songwriter Phil Lam to help a teenage boy with a rare disease, Tsz Kin, ...

We are thrilled that the FDA has recognized the unmet needs in the chronic neutropenia community and granted us Fast Track designation for mavorixafor for the treatment of CN,” said Christophe ...

Skylar Hubbard is battling ultra-rare beta-manosidosis, hoping to find a lasting cure. To do so, her family is working to ...

Dr. Ethel Aguirre Flores broke her first bone before she learned to walk. Since then, she has endured more than 125 other ...

One key finding is that people taking denosumab were five times more likely to develop jaw problems compared to those using ...

Certain medications used in the treatment of bone conditions, particularly when combined with corticosteroids, may ...

Thanks to a global partnership among genetics researchers and the relentless organizing of parents, the five D.C.-area ...

A San Francisco boy with a rare bone marrow disease has been on the waitlist for more than a year. One of his biggest challenges is finding a donor that matches his specific ethnicity: Chinese and ...

Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease that causes human connective tissue to turn into bone. Here's how it works. Qatar pushes back on reports of $400M Boeing jet ...

Once the disease has reached the bone the only option is amputation. "I was able to slightly walk, although the disease had eaten all my toes," Lokonyi, 28, told AFP. She was shunned by the local ...