Complex Biology of Hyperinsulinism May Offer Clues to Better Treatment
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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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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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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.
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Charles Stanley, MD, the founding director of the Congenital Hyperinsulinism Center at CHOP, was presented with a lifetime achievement award by Congenital Hyperinsulinism International (CHI) at the Sugar Soiree in New York City in November.
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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.
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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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At 4 years old, Leila is proof that in some children hyperinsulinism (HI) is transient: She outgrew it.
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Jaylene was born with Beckwith-Wiedemann syndrome (BWS), a rare genetic condition. She had a near-total pancreatectomy at 9 weeks old.
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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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An infant with hyperinsulinism (HI) and Beckwith-Wiedemann syndrome (BWS) faces unique challenges with oral feeding.
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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.