Queen’s University Develops Diagnostic Test for IIH Childhood Disease
A breakthrough in genetic research has uncovered the defect behind a rare hereditary children’s disease that inhibits the body’s ability to break down vitamin D. This discovery has led researchers to develop the first genetic and biochemical tests that positively identify the disease. Idiopathic Infantile Hypercalcemia (IIH) is among the top ten most common inherited… Keep Reading