ReviewAnnals of medicine and surgery (2012)2025
Diverse clinical manifestations and management strategies in autoimmune polyglandular syndrome: a review of cases.
Review in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Distinguishing clinical features of paediatric autoimmune Addison's disease and polyendocrine syndromes: a 15-year single-centre observational study from Baghdad, Iraq.Pediatric endocrinology, diabetes, and metabolism · 2026Observational
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Autoimmune polyglandular syndrome (APS) is a rare autoimmune disease that affects multiple endocrine glands. It can lead to various clinical manifestations. The primary objective of this review was to provide a comprehensive analysis of the clinical features and management strategies used in managing APS, based on a review of case reports. We emphasize disease pattern recognition and detection of atypical clinical signs, as well as the outcomes of various treatment modalities. Case reports from credible journals were searched in PubMed, resulting in a systematic literature review adopting the 2020 Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines. Of the 1173 records identified, 474 remained after duplicates were removed, and 49 full-text articles were reviewed. After further screening based on criteria such as associated disorders, patient age, follow-up, and treatment details, 12 articles were selected for the final analysis. The findings revealed that common endocrine dysfunctions in APS include Addison's disease and hypothyroidism, while non-endocrine manifestations, such as autoimmune encephalitis and pernicious anemia, can also occur. The most frequently adopted strategies were immunosuppressive and hormone therapies. The heterogeneity of APS indicates early diagnosis and individualized treatment strategies. Ultimately, this analysis identifies existing insufficiencies and provides recommendations for formulating standard operating procedures for the treatment of APS.
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What Socratic holds
Registered trials
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 Socratic graph.