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Autoimmune polyglandular syndrome type I. A case report
P Cinaz1, A Bideci, A Haznedaroğlu
1Department of Pediatric Endocrinology, Gazi University Faculty of Medicine, Ankara.
The Turkish Journal of Pediatrics
|April 1, 1997
Summary
Autoimmune Polyglandular Syndrome type I (APS I) is a rare disorder. This case study details a 16-year-old diagnosed with APS I, presenting with hypoparathyroidism, Hashimato
Area of Science:
- Endocrinology
- Immunology
- Genetics
Background:
- Autoimmune Polyglandular Syndrome type I (APS I) is a rare autoimmune disorder.
- Characterized by a triad of hypoparathyroidism (HPT), adrenocortical insufficiency (ACI), and chronic mucocutaneous candidiasis.
- Other endocrine and non-endocrine conditions can be associated with APS I.
Observation:
- A 16-year-old female patient was diagnosed with APS type I.
- The patient presented with HPT, Hashimato's thyroiditis, and ACI.
- She has been monitored for over four years for potential co-occurring disorders.
Findings:
- Diagnosis of APS type I confirmed in a young patient.
- Co-occurrence of HPT, Hashimato's thyroiditis, and ACI in the patient.
- Extended observation period for associated conditions.
Implications:
- Highlights the importance of early diagnosis and comprehensive management of APS I.
- Underscores the potential for diverse clinical presentations and associated conditions.
- Emphasizes the need for long-term monitoring in patients with APS I.