Evidence map›Paper›PMID 41049521›Full record

ArticleClinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology2025

A Japanese infant with fulminant type 1 diabetes with disease-sensitive

Junko Kanno, Hirohito Shima, Miki Kamimura, Akiko Saito-Hakoda, Atsuo Kikuchi

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In one paragraph

Article in Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 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

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Junko KannoDepartment of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Hirohito ShimaDepartment of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Miki KamimuraDepartment of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Akiko Saito-HakodaDepartment of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Atsuo KikuchiDepartment of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fulminant type 1 diabetes mellitus (FT1DM) is a subtype of type 1 diabetes (T1DM) with an acute onset. There are limited reports on FT1DM in pediatric patients. Here, we report the case of a Japanese female infant with FT1DM, representing the youngest female with FT1DM documented to date. The patient was referred to our hospital at 10 mo of age. Although her laboratory findings met the diagnostic criteria for severe diabetic ketoacidosis, her HbA1c level was not excessively high. Anti-glutamic acid decarboxylase and anti-insulinoma-associated protein-2 antibodies were not detected. Test results for insulin autoantibodies were positive. The glucagon stimulation-loading test revealed a C-peptide level of < 0.6 ng/mL. At 8 yr of age, the patient was diagnosed with Graves' disease. Human leukocyte antigen typing and analysis of a single-nucleotide polymorphism (rs3782151) in

Indexed as

CSADfulminant type 1 diabetes mellitusGraves’ diseaseHLA haplotype

Identifiers

PMID41049521
PMCPMC12494394

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.