Format

Send to

Choose Destination

See 1 citation found by title matching your search:

J Community Hosp Intern Med Perspect. 2016 Oct 26;6(5):32983. doi: 10.3402/jchimp.v6.32983. eCollection 2016.

Glucokinase mutation-a rare cause of recurrent hypoglycemia in adults: a case report and literature review.

Author information

1
Department of Internal Medicine, University of Pittsburgh Medical Center, McKeesport, PA, USA; ajalaon@upmc.edu.
2
Department of Internal Medicine, University of Tennessee College of Medicine, Chattanooga, TN, USA.
3
Department of Internal Medicine, University of Pittsburgh Medical Center, McKeesport, PA, USA.

Abstract

BACKGROUND:

Hypoglycemia occurs frequently in patients both in the inpatient and outpatient settings. While most hypoglycemia unrelated to diabetes treatment results from excessive endogenous insulin action, rare cases involve functional and congenital mutations in glycolytic enzymes of insulin regulation.

CASE:

A 21-year-old obese woman presented to the emergency department with complaints of repeated episodes of lethargy, syncope, dizziness, and sweating. She was referred from an outside facility on suspicion of insulinoma, with severe hypoglycemia unresponsive to repeated dextrose infusions. Her plasma glucose was 20 mg/dl at presentation, 44 mg/dl on arrival at our facility, and remained low in spite of multiple dextrose infusions. The patient had been treated for persistent hyperinsulinemic hypoglycemia of infancy at our neonatal facility and 4 years ago was diagnosed as having an activating glucokinase (GCK) mutation. She was then treated with octreotide and diazoxide with improvement in symptoms and blood glucose levels.

CONCLUSION:

Improved diagnostication and management of uncommon genetic mutations as typified in this patient with an activating mutation of the GCK gene has expanded the spectrum of disease in adult medicine. This calls for improved patient information dissemination across different levels and aspects of the health care delivery system to ensure cost-effective and timely health care.

KEYWORDS:

adult; care coordination; care transition; congenital; congenital hyperinsulinism; genetic; glucose; hypoglycemia; low plasma glucose; mutation

Conflict of interest statement

and funding The authors have not received any funding or benefits from industry or elsewhere to conduct this study.

Supplemental Content

Full text links

Icon for PubMed Central
Loading ...
Support Center