Kearns-Sayre syndrome: Omar's Story
After a decade, doctors finally provide answers and treatment for a child with a rare syndrome.
After a decade, doctors finally provide answers and treatment for a child with a rare syndrome.
Ignacio has been a healthy and active kid since he received a liver transplant at CHOP when he was two months old, part of his treatment for a rare form of mitochondrial disease.
Facing a tough diagnosis together, CHOP doctors offer Dakota hope and support, while she helps them learn more about her rare mitochondrial disease.
Ryan, 12, has mitochondrial disorder and eosinophilic esophagitis. With the help of specialists, he’s able to attend classes at school.