Primary hyperparathyroidism in a patient with primary aldosteronism

BMC Research Notes

Tamer Tetiker²  Murat Sert²  Mehtap Evran²  Esma Jamaspishvili¹  Barish Sarıakjali² 

[1] Division of Endocrinology, Department of Internal Medicine, Tbilisi State Medical University, Tbilisi, 0177, Georgia;Division of Endocrinology, Department of Internal Medicine, Cukurova University Medical Faculty, Adana, 01330, Turkey

关键词: Multiple endocrine neoplasia syndromes;    Primary aldosteronism;    Primary hyperparathyroidism;   

Others  :  1231541
DOI  :  10.1186/s13104-015-1271-0

 received in 2015-02-25, accepted in 2015-07-06,  发布年份 2015

【 摘 要 】

Background

Primary hyperparathyroidism is one of the most common causes of hypercalcemia. Inherited forms of primary hyperparathyroidism like Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2a, Hyperparathyroidism-Jaw Tumor Syndrome or isolated familial tumors are not common for our population.

Results

We present a case of primary hyperparathyroidism in a 38-year-old Turkish man with hyperaldosteronism (Conn’s syndrome).

Conclusion

Genetic studies could not reveal any mutation. We could not identify any inherit form of the diseases. We wanted the first-line relatives examination of the suspected gene mutation, but they refused.

【 授权许可】

   
2015 Sarıakjali et al.

【 参考文献 】

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