Neonatal hypercalcemia

J Nephrol. 2003 Jul-Aug;16(4):606-8.

Abstract

The causes of hypercalcemia during the neonatal period are varied. Diagnosis is based on the plasma levels of parathyroid hormone (PTH). (a) PTH in plasma is diminished; exogenous o r endogenous calcium overloading is suspected. (b) PTH in plasma is increased; hyperparathyroidism caused by homozygous or heterozygousloss-of-function mutations in the CaR gene is suspected. (c) PTH i n plasma is normal; low or normal urinary calcium excretion (i.e.relative hypocalciuria) and normal PTH plasma levelsare relevant findings of familial hypocalciuric hypercalcemia (FHH) syndrome.

Publication types

  • Review

MeSH terms

  • Calcium-Binding Proteins / genetics
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Hypercalcemia / epidemiology
  • Hypercalcemia / genetics*
  • Hypercalcemia / physiopathology
  • Hyperparathyroidism / epidemiology
  • Hyperparathyroidism / genetics*
  • Hyperparathyroidism / physiopathology
  • Incidence
  • Infant, Newborn
  • Male
  • Mutation
  • Parathyroid Hormone / blood
  • Parathyroid Hormone / metabolism*
  • Prognosis
  • Risk Assessment
  • Spain / epidemiology

Substances

  • Calcium-Binding Proteins
  • Parathyroid Hormone