Autor: |
Maltese G; Department of Diabetes and Endocrinology Guy's and St Thomas' Hospital NHS Foundation Trust London SE1 7EH UK., Izatt L; Division of Clinical and Molecular Genetics Guy's and St Thomas' Hospital NHS Foundation Trust London SE1 7EH UK., McGowan BM; Department of Diabetes and Endocrinology Guy's and St Thomas' Hospital NHS Foundation Trust London SE1 7EH UK., Hafeez K; Department of Diabetes and Endocrinology Guy's and St Thomas' Hospital NHS Foundation Trust London SE1 7EH UK., Hubbard JG; Department of Diabetes and Endocrinology Guy's and St Thomas' Hospital NHS Foundation Trust London SE1 7EH UK., Carroll PV; Department of Diabetes and Endocrinology Guy's and St Thomas' Hospital NHS Foundation Trust London SE1 7EH UK. |
Jazyk: |
angličtina |
Zdroj: |
Clinical case reports [Clin Case Rep] 2017 Aug 17; Vol. 5 (10), pp. 1587-1590. Date of Electronic Publication: 2017 Aug 17 (Print Publication: 2017). |
DOI: |
10.1002/ccr3.1074 |
Abstrakt: |
We describe a rare case of homozygous inactivating calcium-sensing receptor mutation detected during pregnancy and mimicking primary hyperparathyroidism. In pregnancy, the differential diagnosis of hypercalcaemia requires a cautious approach as physiological changes in calcium homeostasis may mask rare genetic conditions. |
Databáze: |
MEDLINE |
Externí odkaz: |
|
Nepřihlášeným uživatelům se plný text nezobrazuje |
K zobrazení výsledku je třeba se přihlásit.
|