Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3

Familial hypocalciuric hypercalcemia type 3 should be considered as differential diagnosis in patients with suspected primary hyperparathyroidism and/or suspected multiple neoplasia syndrome, as correct diagnosis will spare the patients for going through multiple futile parathyroidectomies and for t...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Clin Case Rep
Egile Nagusiak: Hovden, Silje, Jespersen, Marie Louise, Nissen, Peter H., Poulsen, Per Løgstrup, Rolighed, Lars, Ladefoged, Søren A., Rejnmark, Lars
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: John Wiley and Sons Inc. 2016
Gaiak:
Case Reports
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5054464/
https://ncbi.nlm.nih.gov/pubmed/27761240
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.657
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