Think twice: a rare calcium sensing receptor mutation and a new diagnosis of familial hypocalciuric hypercalcaemia

Autor: Ghusoon Abdulrasool, Louise C H Ciin, Jane J Tellam

Publikováno v: Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2020)

Summary Distinguishing primary hyperparathyroidism (PHPT) from familial hypocalciuric hypercalcaemia (FHH) can be challenging. Currently, 24-h urinary calcium is used to differentiate between the two conditions in vitamin D replete patients, with uri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41b9c3c1bc113f5733344b0aa0b445ca
http://europepmc.org/articles/PMC7354709