Hypercalcemia Report

Dhs. 115.00

Hypercalcemia

The condition of hypercalcemia is characterized by an increase in calcium levels in the blood and is divided into two forms: parathyroid hormone (PTH)-mediated and non-PTH-mediated. PTH, in fact, regulates the concentrations of calcium and phosphorus by acting on the kidneys, bones and intestines. Familial hypocalciuric hypercalcemia is caused by mutations in calcium-sensitive receptors, resulting in an increase in both calcium and PTH and belongs to the first group.

10 genes analyzed


It is recommended if:

Hypercalcemia of genetic origin should be identified in those who are at a young age, have a positive family history for the condition or have had a tumor of the endocrine pancreas, thyroid, pituitary, adrenal gland or jaw bone.


List of main conditions:

  • Hypocalciuric hypercalcemia, type III
  • Hyperparathyroidism-jaw tumor syndrome
  • Parathyroid adenoma with cystic changes
  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • Investigates SNP and Indel mutations up to 150 bp

Simple workflow

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