One in a million
A young chlld and her family face an extremely rare and unpredictable condition.
A young chlld and her family face an extremely rare and unpredictable condition.
Advances in medical genetics and personalized medicine are opening new vistas in diagnosis and treatment.
Genetic testing helps a Michigan mom and dad find answers to their baby's rare condition.
The Gashi family, of Michigan, traveled far in their quest for answers to their daughter’s mysterious illness. They found success right here at home.
In the quest to treat their 6-year-old boy's rare disease, a California couple finds answers in West Michigan.
For a Michigan couple eager to help their son, genetics research is lighting the path ahead.
An energetic 6-year-old is leading the way in treatment for a rare genetic mutation.
Daxton, 2, and Sawyer, 4, battle a rare genetic disease with a team of specialists and the calming power of music.
Genetic testing helps the family of a Michigan boy dig deeper into his unique health challenges.
Genetic testing that pinpointed a rare disorder helped a Michigan couple give their daughter the tools she needs to blossom.
Addison Weith’s genes put her at risk for health troubles. Her family’s vigilance during the pandemic has kept her healthy for the longest stretch ever.
To dodge genetic risks, a Michigan teen opts for thyroid surgery. Her family is glad she did.