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  1. 21-Hydroxylase Deficient Congenital Adrenal Hyperplasia Due to Maternal Uniparental Isodisomy

    Published in Case Reports in Endocrinology (2026)
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  2. High-Risk Pregnancy Associated With Maternal Hypoparathyroidism and Medium-Chain Acyl-CoA Dehydrogenase Deficiency

    Published in Case Reports in Endocrinology (2026)
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  3. Recognition of Macrocephaly for Early Detection of Cowden Syndrome With Differentiated Thyroid Cancer and Melanoma

    Published in Case Reports in Endocrinology (2026)
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  4. Correction to “A Decade With Sheehan’s Syndrome: A Case Report and Personal Experience”

    Published in Case Reports in Endocrinology (2026)
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  5. Timing of Denosumab Therapy in Relation to Parathyroidectomy in the Setting of Primary Hyperparathyroidism: Case Report

    Published in Case Reports in Endocrinology (2026)
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  6. DUOXA2 Variants as an Underrecognized Cause of Diffuse Goiter: A Euthyroid Adult Case Responsive to Levothyroxine

    Published in Case Reports in Endocrinology (2026)
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  7. Coexisting ADAR and TSHB Mutations in an Infant With Retinal Detachment and Transient Cardiomyopathy

    Published in Case Reports in Endocrinology (2026)
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  8. Triple Trouble: Early Clues in the Diagnosis of Allgrove Syndrome: A Case Report

    Published in Case Reports in Endocrinology (2026)
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  9. A Modern-Day Captain Charles Martell: Catastrophic Skeletal Manifestations of Primary Hyperparathyroidism

    Published in Case Reports in Endocrinology (2026)
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  10. Severe Transient Central Diabetes Insipidus After Pituitary Adenoma Removal With Peak Urine Output of 33.5 L in 24 h

    Published in Case Reports in Endocrinology (2026)
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  11. Primary Aldosteronism Presenting as Dropped Head Syndrome With Hypokalemic Rhabdomyolysis: A Case Report

    Published in Case Reports in Endocrinology (2026)
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  12. Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency Presented With Leydig Cell Tumor and Testicular Adrenal Rest Tumors: A Case Report

    Published in Case Reports in Endocrinology (2026)
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  13. Acute Kidney Injury and Nephrotic-Range Proteinuria as Initial Presentation of Pheochromocytoma: A Case Report

    Published in Case Reports in Endocrinology (2026)
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  14. Denys-Drash Syndrome by WT1 Gene: Clinical Variability and Management Challenges in Two Saudi Infants

    Published in Case Reports in Endocrinology (2026)
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  15. Partial Horner’s Syndrome Following Thyroidectomy Without Lateral Neck Dissection: A Rare Case Report and Literature Review

    Published in Case Reports in Endocrinology (2026)
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  16. A Rare Primary Adrenal Malignancy Manifesting as a Hemorrhagic Mass: Case Report and Literature Review

    Published in Case Reports in Endocrinology (2026)
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  17. Thyroid Storm at Sea: A Case Report of Algae-Induced Thyrotoxicosis

    Published in Case Reports in Endocrinology (2026)
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  18. Mild Autonomous Cortisol Secretion in Context of Bilateral Macronodular Adrenocortical Disease due to ARMC5 Mutation: A Rare Familial Case

    Published in Case Reports in Endocrinology (2026)
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  19. Cushing Syndrome Secondary to Adrenal Adenoma Diagnosed Following Unsuccessful Bariatric Surgery: A Case Report

    Published in Case Reports in Endocrinology (2026)
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