2SNP and 4SNP

Carried out in order to reliably diagnose autosomal recessive inherited metabolic disease, hemochromatosis. This disease is one of the most common hereditary diseases, but, unfortunately, often have nonspecific symptoms common to many different diseases. Diagnosis of the disease is often difficult. Most accurate and fastest haemochromatosis confirmed by genetic testing.
2SNP investigation determined the two most common disease in determining the HFE gene mutations (C282Y and H63D), found in 90 percent of all patients. 4SNP without C282Y and H63D, HFE gene analyzes and the reduction in the frequency of mutations, e.g. 65C and E168X.
In familial predisposition, identification of mutations even in early childhood enables start-savailaikį preventative treatment and protection from long disease complications.

More information: www.euroimmun.com