A case report of familial type 2 diabetes mellitus combined with hypothyroidism and multiple autoimmune diseases

Gene mutations in the Janus kinase/signal transducer and activator of transcription signaling (JAK/STAT) pathway can promote the occurrence of type 2 diabetes mellitus (T2DM) and autoimmune diseases. We report on two patients with T2DM (a mother and her adult son) with concomitant Hashimoto's thyroiditis and autoimmune diseases. The son was diagnosed with systemic sclerosis and antiphospholipid syndrome, while the mother was diagnosed with primary biliary cholangitis. Both diagnoses occurred simultaneously. These cases highlight that, in clinical practice, careful symptom assessment, thorough history-taking, standardized physical examination, and obtaining a detailed family history are important. This reduces the misdiagnosis and missed diagnosis rates, enabling early diagnosis and treatment, thereby improving patient outcomes. While genetic testing was not performed in these two patients, this represents a potential direction for future research.

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Publication Details

Journal
Frontiers in Endocrinology
Published
2025-08-04
DOI
https://doi.org/10.3389/fendo.2025.1599546
Primary Topic
Genetic factors in colorectal cancer
Type
article
Field-Weighted Citation Impact
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article

A case report of familial type 2 diabetes mellitus combined with hypothyroidism and multiple autoimmune diseases

Xulong Lai, Yang Yang, Xin Su, Yan Qu et al.
Frontiers in Endocrinology
Genetic factors in colorectal cancer
article

A case report of familial type 2 diabetes mellitus combined with hypothyroidism and multiple autoimmune diseases

Xulong Lai, Yang Yang, Xin Su, Yan Qu, Haotian Jiang
article en

Abstract

Gene mutations in the Janus kinase/signal transducer and activator of transcription signaling (JAK/STAT) pathway can promote the occurrence of type 2 diabetes mellitus (T2DM) and autoimmune diseases. We report on two patients with T2DM (a mother and her adult son) with concomitant Hashimoto's thyroiditis and autoimmune diseases. The son was diagnosed with systemic sclerosis and antiphospholipid syndrome, while the mother was diagnosed with primary biliary cholangitis. Both diagnoses occurred simultaneously. These cases highlight that, in clinical practice, careful symptom assessment, thorough history-taking, standardized physical examination, and obtaining a detailed family history are important. This reduces the misdiagnosis and missed diagnosis rates, enabling early diagnosis and treatment, thereby improving patient outcomes. While genetic testing was not performed in these two patients, this represents a potential direction for future research.

Frontiers in EndocrinologyVol. 16
Wuhan University of Technology (CN), Wuhan University of Science and Technology (CN)
Good health and well-being
Openalex Percentile: Top 72%
Genetic factors in colorectal cancer
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