Coexistence of T1DM and GCK-MODY: Case Report and Literature Review

Coexistence of Type 1 diabetes mellitus (T1DM) with glucokinase maturity-onset diabetes of the young (GCK-MODY) is extremely rare. Herein, we reported a case, conducted a systematic review and summarized the other reported cases to enhance the awareness of this rare diabetes subtype. An 11-year-old boy was presented with polydipsia, polyuria, and weight loss. He was diagnosed with T1DM based on significant hyperglycemia, decreased C-peptide levels, and positive diabetes-related antibodies. Genetic testing revealed that both the patient and his father carried a heterozygous mutation in the GCK gene. Due to the coexistence of GCK-MODY, the patient experienced difficulties in glycemic control and frequent hypoglycemia during insulin therapy. The patient's father gradually reduced and discontinued insulin treatment after genetic test. In clinical practice, the possibility of overlapping diabetes types should be highly emphasized. Genetic testing should be performed to optimize treatment plans and improve patient outcomes.

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Publication Details

Journal
Journal of Clinical Research in Pediatric Endocrinology
Published
2025-10-28
DOI
https://doi.org/10.4274/jcrpe.galenos.2025.2025-7-18
Citations
1
Primary Topic
Connective tissue disorders research
Type
article
Field-Weighted Citation Impact
1.82
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article

Coexistence of T1DM and GCK-MODY: Case Report and Literature Review

Di Wu, Yanmei Sang, Congli Chen, Yuqi Miao et al.
1 citations
Journal of Clinical Research in Pediatric Endocrinology
Connective tissue disorders research
1.82
article

Coexistence of T1DM and GCK-MODY: Case Report and Literature Review

Di Wu, Yanmei Sang, Congli Chen, Yuqi Miao, Yurong Piao
article en
1 citations

Abstract

Coexistence of Type 1 diabetes mellitus (T1DM) with glucokinase maturity-onset diabetes of the young (GCK-MODY) is extremely rare. Herein, we reported a case, conducted a systematic review and summarized the other reported cases to enhance the awareness of this rare diabetes subtype. An 11-year-old boy was presented with polydipsia, polyuria, and weight loss. He was diagnosed with T1DM based on significant hyperglycemia, decreased C-peptide levels, and positive diabetes-related antibodies. Genetic testing revealed that both the patient and his father carried a heterozygous mutation in the GCK gene. Due to the coexistence of GCK-MODY, the patient experienced difficulties in glycemic control and frequent hypoglycemia during insulin therapy. The patient's father gradually reduced and discontinued insulin treatment after genetic test. In clinical practice, the possibility of overlapping diabetes types should be highly emphasized. Genetic testing should be performed to optimize treatment plans and improve patient outcomes.

Journal of Clinical Research in Pediatric Endocrinology
Capital Medical University (CN), Beijing Children’s Hospital (CN)
Openalex Percentile: Top 12%
Connective tissue disorders research
1.82
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Coexistence of T1DM and GCK-MODY: Case Report and Literature Review — Di Wu, Yanmei Sang, et al. · Journal of Clinical Research in Pediatric Endocrinology (2025) | TGRS Research Map | TGRS