Hyperinsulinemic Hypoglycemia and Growth Hormone Deficiency Secondary to 20p11 Deletion

Author:

Wee Erica12ORCID,Herriges John23ORCID,Dileepan Kavitha12ORCID,Tsai Sarah L.12ORCID,Alaimo Joseph T.23ORCID,Paprocki Emily12ORCID

Affiliation:

1. Division of Pediatric Endocrinology and Diabetes, Children’s Mercy Kansas City, Kansas City, MO, USA

2. University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA

3. Department of Pathology and Laboratory Medicine, Children’s Mercy Kansas City, Kansas City, MO, USA

Abstract

Hypoglycemia is concerning for neurological complications in infants and children. Determining the cause of hypoglycemia is essential in providing appropriate treatment. Hyperinsulinism and growth hormone deficiency are known causes of hypoglycemia but are not commonly found together. We report a 4-month-old boy who presented with severe hypoglycemia and was found to have both hyperinsulinism and growth hormone deficiency. Treatment with both recombinant human growth hormone and diazoxide led to blood glucose normalization. Subsequently, he was found to have a genetic diagnosis of 20p11.22p11.21 deletion. 20p11 deletions have been associated with hypopituitarism, most commonly seen in growth hormone deficiency causing hypoglycemia. This case is one of a few to report hyperinsulinism as a manifestation of this deletion.

Publisher

Hindawi Limited

Subject

Endocrinology, Diabetes and Metabolism

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Factors associated with neonatal hyperinsulinemic hypoglycemia, a case-control study;Journal of Pediatric Endocrinology and Metabolism;2024-01-19

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