Thousands of times per year, a family’s moment of joy turns to unexpected grief. A seemingly healthy infant stops smiling or ...

Jeff and Deena Leider are pushing federal officials to expand access to a treatment for their two sons' rare disease.

Some 25 million Americans live with rare genetic diseases — that’s nearly 1 in 13. More than half are children. The path to discovering what the condition is, and finding treatments, can take years.

GOLDSBORO, N.C. (WITN) - A Goldsboro family is sharing their story and asking for community support as they raise their two-year-old son, diagnosed with a rare genetic disorder. Declan Newberry was ...

KUALA LUMPUR - A recent viral story on social media tells of a fair-skinned baby with long eyelashes who, at first glance, appears no different from any other infant. Few would have guessed that the ...

Disclaimer: This article is for informational and educational purposes only and should not be considered medical advice. Anyone concerned about symptoms or health conditions should consult a qualified ...

LOUISVILLE, Ky. (WAVE) - Carter Twigg held her son Owen for the last time on Sept. 29, 2023, after he went to sleep and didn’t wake up. Owen Twigg was born with a cleft lip and palate and complex ...

Doctors at Artemis Hospitals have successfully treated India's first MYSM1-related bone marrow failure syndrome case using a ...

KSHB 41 reporter Olivia Acree covers portions of Johnson County, Kansas. A viewer reached out to KSHB about this story, so Olivia sat down with the family. Share your story idea with Olivia. We are ...

Researchers led by the University of Vienna and Liège University Hospital Centre have identified genetic variants associated with a rare inherited growth disorder in two prehistoric individuals who ...