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Primary hyperparathyroidism in a patient with primary aldosteronism

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...

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Detalles Bibliográficos
Autores principales: Sarıakjali, Barish, Jamaspishvili, Esma, Evran, Mehtap, Sert, Murat, Tetiker, Tamer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508971/
https://www.ncbi.nlm.nih.gov/pubmed/26198579
http://dx.doi.org/10.1186/s13104-015-1271-0
Descripción
Sumario: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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-015-1271-0) contains supplementary material, which is available to authorized users.