Evidence map›Paper›PMID 41480612›Full record

ArticleWorld journal of diabetes2025

Clinical and genetic characteristics of young-onset diabetes with concurrent mitochondrial m.3243A>G and

Xiao-Dan Che, Zheng-Liang Wei, Wuriliga Gong, Ling Qin, Shuang Liu, Yuan-Hui Jin, He-Yuan Wang

Abstract readCase Reports
PubMed Full text at PMC Publisher
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Article in World journal of diabetes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Xiao-Dan CheDepartment of Endocrinology, Meihekou Central Hospital, Meihekou 135000, Jilin Province, China.
Zheng-Liang WeiDepartment of Endocrinology and Metabolism, The First Hospital of Jilin University, Changchun 130000, Jilin Province, China.
Wuriliga GongDepartment of Endocrinology and Metabolism, The First Hospital of Jilin University, Changchun 130000, Jilin Province, China.
Ling QinDepartment of Endocrinology, Meihekou Central Hospital, Meihekou 135000, Jilin Province, China.
Shuang LiuDepartment of Endocrinology, Meihekou Central Hospital, Meihekou 135000, Jilin Province, China.
Yuan-Hui JinDepartment of Endocrinology, Meihekou Central Hospital, Meihekou 135000, Jilin Province, China.
He-Yuan WangDepartment of Endocrinology and Metabolism, The First Hospital of Jilin University, Changchun 130000, Jilin Province, China. wangheyuan@jlu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOnly a few cases of diabetes mellitus with concurrent mutations in the mitochondrial CASE SUMMARY: A 30-year-old man, diagnosed with diabetic ketoacidosis six years earlier, presented with poor response to insulin therapy (glycated hemoglobin, 15.35%), marked wasting (body mass index: 15.06 kg/m

conclusionThis case highlights the genetic heterogeneity of monogenic diabetes and expands the known mutational spectrum. Comprehensive genetic testing is recommended to enhance diagnostic accuracy in cases of suspected monogenic diabetes.

Indexed as

Case reportDual mutationsGenetic heterogeneityMonogenic diabetesMutational spectrumPrecise diagnosis

Identifiers

PMID41480612
PMCPMC12754127

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