CHOP’s Congenital Hyperinsulinism Center Celebrates 20 Years and 500 Surgeries
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The center offers evaluation, diagnosis, treatment, and follow-up care for children with this life-threatening condition.
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The center offers evaluation, diagnosis, treatment, and follow-up care for children with this life-threatening condition.
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CHOP’s groundbreaking expertise in treating children with congenital hyperinsulinism (HI) began more than 50 years ago and draws patients from all over the world.
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Two generations of the Parkes family have come to Children’s Hospital of Philadelphia for treatment for hyperinsulinism (HI). They’ve seen and experienced breakthroughs in HI care firsthand.
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Leaders of the HI Center at CHOP remember two decades of advancements in care for children with HI.
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Children with congenital hyperinsulinism (HI) may be at risk for exocrine pancreatic insufficiency, which affects the ability of the pancreas to function properly.
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Patients share their experiences of growing up with HI during the 2016 Congenital Hyperinsulinism Family Conference in Philadelphia.
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Charles A. Stanley, MD, received the Judson J. Van Wyk Prize, the most prestigious award given by the Pediatric Endocrine Society.
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Studying cells from children born with hyperinsulinism, CHOP experts discover events at the cellular level that may lead to new treatments for this rare disease.
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CHOP's Congenital Hyperinsulism Center taps David R. Langdon, MD, to be director of inpatient service as former director Andrew Palladino, MD, moves to HI outpatient clinic.
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CHOP has found that an investigational drug could point to the first potential medical treatment for children with a type of HI.