Caring for a Rare Variation of a Rare Disease
CHOP not only diagnosed Amelia’s extremely uncommon condition, it had the experts to treat her.
Our team of pediatric endocrinologists, surgeons, radiologists, pathologists, anesthesiologists, advanced practice nurses, nurses, social workers, genetic counselors, psychologists, researchers, speech and feeding therapists, and dietitians work together to provide specialized and seamless care.
CHOP not only diagnosed Amelia’s extremely uncommon condition, it had the experts to treat her.
Caring for three siblings with hyperinsulinism — and keeping their blood sugar in the safe range — calls for creativity and guidance from CHOP.
Being part of a clinical trial as a patient of the HI Center research gave Nico the independence to be a normal kid and still safely manage his hyperinsulinism.
Grandfather, mom and granddaughter have all been treated at CHOP for congenital hyperinsulinism (HI). This family’s history shows the evolution of HI care.
Eliza’s family brought her to CHOP for its expertise in hyperinsulinism. She became the 600th patient to have pancreas surgery and went home cured.
After three months of searching for answers, Omar’s family found a diagnosis — and hope, at Children’s Hospital of Philadelphia.
When a rare disorder was diagnosed in two of their children, the Linares family found hope and expertise at CHOP.
Endocrinologists in New York didn’t have the knowledge of hyperinsulinism to help Dominique, 30, so she came to CHOP for treatment that controlled her HI.
Much has been learned about hyperinsulinism/hyperammonemia since Daniel first had severe low blood sugar as a baby. A new clinic as CHOP can help improve symptoms.
A diagnosis of Kabuki syndrome connected all of Amelia’s symptoms, and CHOP has experts to care for each and every condition.