Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation.
Manuela CapozzaIolanda ChinellatoVito GuarnieriNatascia Di LorgiMaria AccadiaCristina TraggiaiGirolamo MattioliAntonio Di MauroNicola LaforgiaPublished in: BMC pediatrics (2018)
This case of NSHPT suggests that a near-miss event, labelled as a possible case of SIDS, could also be due to severe hypercalcemia and evidentiates the difficulties of the neonatal management of NSHPT. Furthermore, the identification of the specific CaSR mutation provides the substrate for prenatal diagnosis.