Hyperinsulinemic Hypoglycemia and Growth Hormone Deficiency Secondary to 20p11 Deletion.

IF 0.9 Q4 ENDOCRINOLOGY & METABOLISM
Case Reports in Endocrinology Pub Date : 2023-06-26 eCollection Date: 2023-01-01 DOI:10.1155/2023/8658540
Erica Wee, John Herriges, Kavitha Dileepan, Sarah L Tsai, Joseph T Alaimo, Emily Paprocki
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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.

Abstract Image

继发于 20p11 缺失的高胰岛素血症和生长激素缺乏症
低血糖会导致婴幼儿神经系统并发症。确定低血糖的原因对于提供适当的治疗至关重要。高胰岛素血症和生长激素缺乏症是低血糖症的已知病因,但两者同时出现并不常见。我们报告了一名 4 个月大的男孩,他出现了严重的低血糖症,并同时患有胰岛素分泌过多症和生长激素缺乏症。使用重组人生长激素和地佐唑治疗后,血糖恢复正常。随后,他被确诊为 20p11.22p11.21 缺失。20p11 缺失与垂体功能减退症有关,最常见于生长激素缺乏引起的低血糖。本病例是少数几个报告高胰岛素血症为该缺失表现的病例之一。
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来源期刊
Case Reports in Endocrinology
Case Reports in Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.10
自引率
0.00%
发文量
45
审稿时长
13 weeks
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