Could OMRF provide the answers Melissa Cain so desperately sought about her daughter’s illness?
spondyloepiphyseal dysplasia
Oklahoma teen lives with unique skeletal disorder
Sydney Rutz is one in five billion.
1 In 5 Billion
There are people who suffer from rare diseases. And then there’s Sydney Rutz, who has a genetic condition never before identified–until a group of OMRF scientists took on her case.
