GCM2 mutation in primary hyperparathyroidism - A Case Report
Primary hyperparathyroidism is a common endocrine disorder. It is characterised by elevated parathyroid hormone (PTH) level causing hypercalcemia. 90-95% of cases have a spontaneous cause, with the remaining 5-10% having a genetic basis. On routine examination, a 47-year-old patient was found to ha...
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| Principais autores: | , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Kazimierz Wielki University
2024-05-01
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| Serija: | Journal of Education, Health and Sport |
| Teme: | |
| Online dostop: | https://apcz.umk.pl/JEHS/article/view/50880 |
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