Glucokinase maturity-onset diabetes of the young as a mimicker of stress hyperglycemia: a case report.

IF 1 Q4 ENDOCRINOLOGY & METABOLISM Clinical Pediatric Endocrinology Pub Date : 2023-01-01 DOI:10.1297/cpe.2022-0024
Yoshitaka Nakasato, Shintaro Terashita, Shohei Kusabiraki, Sadashi Horie, Takuya Wada, Motokazu Nakabayashi, Megumi Nakamura, Tohru Yorifuji
{"title":"Glucokinase maturity-onset diabetes of the young as a mimicker of stress hyperglycemia: a case report.","authors":"Yoshitaka Nakasato, Shintaro Terashita, Shohei Kusabiraki, Sadashi Horie, Takuya Wada, Motokazu Nakabayashi, Megumi Nakamura, Tohru Yorifuji","doi":"10.1297/cpe.2022-0024","DOIUrl":null,"url":null,"abstract":"Abstract. Febrile seizures are frequently accompanied by stress-induced hyperglycemia. Herein, we report the case of a 1.5-yr-old girl with hyperglycemia during febrile seizures who was subsequently diagnosed with glucokinase (GCK) maturity-onset diabetes of the young (MODY), considering its distinction from stress hyperglycemia. Following the development of febrile seizures owing to adenovirus infection, the patient presented a casual blood glucose level was 185 mg/dL. She had a multigenerational family history of diabetes and a hemoglobin A1c (HbA1c) level of 6.4%. Owing to the persistent glucose intolerance until the age of 5 years, genetic testing was performed, which revealed a heterozygous mutation in GCK, and the patient was diagnosed with GCK-MODY. Precise diagnosis of GCK-MODY individuals is important to avoid administering unnecessary antidiabetic medications. Even during hyperglycemia under stress, multigenerational diabetes and mildly elevated HbA1c levels can suggest GCK-MODY.","PeriodicalId":10678,"journal":{"name":"Clinical Pediatric Endocrinology","volume":null,"pages":null},"PeriodicalIF":1.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/0e/05/cpe-32-072.PMC9887293.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Pediatric Endocrinology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1297/cpe.2022-0024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 1

Abstract

Abstract. Febrile seizures are frequently accompanied by stress-induced hyperglycemia. Herein, we report the case of a 1.5-yr-old girl with hyperglycemia during febrile seizures who was subsequently diagnosed with glucokinase (GCK) maturity-onset diabetes of the young (MODY), considering its distinction from stress hyperglycemia. Following the development of febrile seizures owing to adenovirus infection, the patient presented a casual blood glucose level was 185 mg/dL. She had a multigenerational family history of diabetes and a hemoglobin A1c (HbA1c) level of 6.4%. Owing to the persistent glucose intolerance until the age of 5 years, genetic testing was performed, which revealed a heterozygous mutation in GCK, and the patient was diagnosed with GCK-MODY. Precise diagnosis of GCK-MODY individuals is important to avoid administering unnecessary antidiabetic medications. Even during hyperglycemia under stress, multigenerational diabetes and mildly elevated HbA1c levels can suggest GCK-MODY.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
葡萄糖激酶成熟型糖尿病的年轻人作为模拟应激性高血糖:一个案例报告。
热性惊厥常伴有应激性高血糖。在此,我们报告一例1.5岁的女孩在热性惊厥期间出现高血糖,随后被诊断为葡萄糖激酶(GCK)成熟型糖尿病(MODY),考虑到其与应激性高血糖的区别。在腺病毒感染引起的发热性惊厥发生后,患者的血糖水平为185 mg/dL。她有多代糖尿病家族史,血红蛋白A1c (HbA1c)水平为6.4%。由于持续葡萄糖耐受不良直到5岁,进行基因检测,发现GCK杂合突变,诊断为GCK- mody。准确诊断GCK-MODY个体对于避免使用不必要的抗糖尿病药物非常重要。即使在应激下的高血糖,多代糖尿病和轻度升高的HbA1c水平也可能提示GCK-MODY。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Clinical Pediatric Endocrinology
Clinical Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.40
自引率
7.10%
发文量
34
期刊最新文献
A novel SOX2 frameshift pathogenic variant located in the transactivation domain in a male infant with hypogonadotropic hypogonadism. CHARGE syndrome in a child with a CHD7 variant and a novel pathogenic SOX2 variant: A case report. Familial and early recurrent pheochromocytoma in a child with a novel in-frame duplication variant of VHL. Hearing loss with two pathogenic SLC26A4 variants and positive thyroid autoantibody: A case report. Initial clinical manifestations in a young male with RFX6-variant-associated diabetes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1