Autoimmune Polyglandular Syndrome Type 2 Latest Advances

Oral and Craniofacial Development and Immunology.

Journal: Advances in experimental medicine and biology

Published: November 12, 2025

Overcoming genetic drivers in alopecia areata: Hair regrowth in a patient with AIRE gene mutation (APECED syndrome) treated with ruxolitinib.

Journal: Clinical and experimental dermatology

Published: November 03, 2025

Multiple episodes of paediatric Clostridioides difficile infection (pCDI) in the context of autoimmune polyendocrine syndrome type 1.

Journal: BMJ case reports

Published: October 27, 2025

A Polyendocrine Puzzle: Unravelling Schmidt Syndrome (Autoimmune Polyendocrine Syndrome Type II) Presenting in Crisis.

Journal: Cureus

Published: October 17, 2025

A Rare Autoimmune Quartet: Immune Thrombocytopenia in a Patient with Autoimmune Polyglandular Syndrome Type 3.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: September 25, 2025

Autoimmune Polyglandular Syndrome Type 2 With Hurthle Cell Adenoma: A Rare Association.

Journal: Cureus

Published: September 22, 2025

Head and Neck Malignancies in Autoimmune Polyendocrine Syndrome Type 1 (APS-1/APECED): A Scoping Review of Molecular Pathogenesis, Clinical Features, and Outcomes.

Journal: International journal of molecular sciences

Published: August 30, 2025

Slow Evolution of Non-Familial Autoimmune Polyglandular Syndrome Type II in A 54-Year-Old Female, First Presenting with Addison's Disease, then Hashimoto's Thyroiditis, which then Transitioned to Graves' Disease and then the Development of Type 1 Diabetes.

Journal: European journal of case reports in internal medicine

Published: August 18, 2025

A rare case of autoimmune polyglandular syndrome type 2 in an elderly patient

Journal: Medicina

Published: August 12, 2025

Autoimmune Polyglandular Syndrome Type 3 and Overlapping Autoimmune Endocrinopathies: A Case Report.

Journal: Cureus

Published: July 23, 2025

Balancing IL-17-mediated protection and IFN-γ-driven pathology at mucocutaneous barriers.

Journal: Trends in immunology

Published: July 22, 2025

Diagnostic clues in patients with clinical malabsorption and pathological small intestinal villous atrophy: Immune-mediated type and beyond.

Journal: World journal of gastroenterology

Published: July 21, 2025

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Oral and Craniofacial Development and Immunology.

Oral and Craniofacial Development and Immunology.

Overcoming genetic drivers in alopecia areata: Hair regrowth in a patient with AIRE gene mutation (APECED syndrome) treated with ruxolitinib.

Overcoming genetic drivers in alopecia areata: Hair regrowth in a patient with AIRE gene mutation (APECED syndrome) treated with ruxolitinib.

Multiple episodes of paediatric Clostridioides difficile infection (pCDI) in the context of autoimmune polyendocrine syndrome type 1.

Multiple episodes of paediatric Clostridioides difficile infection (pCDI) in the context of autoimmune polyendocrine syndrome type 1.

A Polyendocrine Puzzle: Unravelling Schmidt Syndrome (Autoimmune Polyendocrine Syndrome Type II) Presenting in Crisis.

A Polyendocrine Puzzle: Unravelling Schmidt Syndrome (Autoimmune Polyendocrine Syndrome Type II) Presenting in Crisis.

A Rare Autoimmune Quartet: Immune Thrombocytopenia in a Patient with Autoimmune Polyglandular Syndrome Type 3.

A Rare Autoimmune Quartet: Immune Thrombocytopenia in a Patient with Autoimmune Polyglandular Syndrome Type 3.

Autoimmune Polyglandular Syndrome Type 2 With Hurthle Cell Adenoma: A Rare Association.

Autoimmune Polyglandular Syndrome Type 2 With Hurthle Cell Adenoma: A Rare Association.

Head and Neck Malignancies in Autoimmune Polyendocrine Syndrome Type 1 (APS-1/APECED): A Scoping Review of Molecular Pathogenesis, Clinical Features, and Outcomes.

Head and Neck Malignancies in Autoimmune Polyendocrine Syndrome Type 1 (APS-1/APECED): A Scoping Review of Molecular Pathogenesis, Clinical Features, and Outcomes.

Slow Evolution of Non-Familial Autoimmune Polyglandular Syndrome Type II in A 54-Year-Old Female, First Presenting with Addison's Disease, then Hashimoto's Thyroiditis, which then Transitioned to Graves' Disease and then the Development of Type 1 Diabetes.

Slow Evolution of Non-Familial Autoimmune Polyglandular Syndrome Type II in A 54-Year-Old Female, First Presenting with Addison's Disease, then Hashimoto's Thyroiditis, which then Transitioned to Graves' Disease and then the Development of Type 1 Diabetes.

A rare case of autoimmune polyglandular syndrome type 2 in an elderly patient

A rare case of autoimmune polyglandular syndrome type 2 in an elderly patient

Autoimmune Polyglandular Syndrome Type 3 and Overlapping Autoimmune Endocrinopathies: A Case Report.

Autoimmune Polyglandular Syndrome Type 3 and Overlapping Autoimmune Endocrinopathies: A Case Report.

Balancing IL-17-mediated protection and IFN-γ-driven pathology at mucocutaneous barriers.

Balancing IL-17-mediated protection and IFN-γ-driven pathology at mucocutaneous barriers.

Diagnostic clues in patients with clinical malabsorption and pathological small intestinal villous atrophy: Immune-mediated type and beyond.

Diagnostic clues in patients with clinical malabsorption and pathological small intestinal villous atrophy: Immune-mediated type and beyond.