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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Clin Case Rep
Huvudupphovsmän: Hovden, Silje, Jespersen, Marie Louise, Nissen, Peter H., Poulsen, Per Løgstrup, Rolighed, Lars, Ladefoged, Søren A., Rejnmark, Lars
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2016
Ämnen:
Case Reports
Länkar: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
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk