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Recurrent Hypoglycemia Secondary to Insulinoma in an Adult With Beckwith-Wiedemann Syndrome. JCEM Case Rep 2023 May;1(3):luad062

Date

11/01/2023

Pubmed ID

37908580

Pubmed Central ID

PMC10580426

DOI

10.1210/jcemcr/luad062

Abstract

Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder characterized by genetic and epigenetic changes on the chromosome 11p15.5 region, which includes genes that are important for fetal and postnatal growth. Children with BWS have a higher chance of having hypoglycemia, hyperinsulinemia, and malignancies early in life, although hypoglycemia caused by an insulinoma that develops later in life has not been reported. We describe the diagnosis of insulinoma in a 53-year-old man with BWS in this case report. This is the first case report of insulinoma in an adult with this syndrome.

Author List

Akcan T, Shariff JRR

Author

Julia Rose Shariff MD Assistant Professor in the Medicine department at Medical College of Wisconsin