Congenital Hyperinsulinism Center News and Updates

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CHOP Article Highlights Three Novel Cases of HNF HI

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Read a brief description about three novel cases of HI caused by mutations in the MODY (maturity-onset diabetes of youth) genes, HNF1A and HNF4A. Two of the cases are the first to report HNF1A mutations as a cause of congenital HI.

Near-total Pancreatectomy Means Eventual Diabetes

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CHOP researchers, led by endocrinologists Katherine Lord, MD, and Diva D. De León-Crutchlow, MD, MSCE, studied the outcomes of 121 patients who had undergone a pancreatectomy. They found that 36 percent later developed diabetes.

HI Center Names New Director of Inpatient Care

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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.

Sometimes, HI Can Fade Away

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At 4 years old, Leila is proof that in some children hyperinsulinism (HI) is transient: She outgrew it.

Focal vs. Diffuse Patients: Comparing Outcomes

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Researchers at CHOP’s HI Center conducted a study comparing the clinical features, treatments and short-term outcomes of children with HI who underwent pancreatectomies.


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