HI Hope

Most Recent Articles

CHOP’s HI Team Leading Research Nationally

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Our HI team has been busy continuing to pave the way to improve the diagnosis, treatment and outcomes for children with hyperinsulinism through discovery and innovation.

The Ups and Downs of Living with HI

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Patients share their experiences of growing up with HI during the 2016 Congenital Hyperinsulinism Family Conference in Philadelphia.

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.

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.