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Clinical and outcome comparison of genetically positive vs. negative patients in a large cohort of suspected familial hypocalciuric hypercalcemia.

Queralt Asla RocaHelena SardàNúria SeguíGuillermo Martínez de PinillosIsabel Mazarico-AltisentIsmael CapelJosé RivesJavier SuárezVerónica Ávila-RubioManuel Munoz-TorresIgnasi SaigíNuria PalaciosEulàlia UrgellSusan M WebbMercè FernándezJosep OriolaMireia MoraMireia TondoAnna Aulinas
Published in: Endocrine (2023)
The combination of magnesium and a positive family history offered a good diagnostic accuracy to predict a positive genetic result. Therefore, the inclusion of magnesium measurement in the routine evaluation of patients with suspected FHH might provide insight into the identification of a positive genetic result of any of the CaSR-related genes.
Keyphrases
  • end stage renal disease
  • chronic kidney disease
  • newly diagnosed
  • genome wide
  • ejection fraction
  • prognostic factors
  • dna methylation
  • copy number
  • early onset
  • patient reported outcomes