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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...
Autores principales: | Hovden, Silje, Jespersen, Marie Louise, Nissen, Peter H., Poulsen, Per Løgstrup, Rolighed, Lars, Ladefoged, Søren A., Rejnmark, Lars |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054464/ https://www.ncbi.nlm.nih.gov/pubmed/27761240 http://dx.doi.org/10.1002/ccr3.657 |
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