Hemochromatosis
Hereditary hemochromatosis (HH) is a recessive genetic disorder characterized by an increased intestinal iron absorption resulting in systemic iron overload, especially in the liver, pancreas, joints and testes. If untreated, HH can cause liver fibrosis, cirrhosis and hepatocellular carcinoma. HH is commonly caused by certain variants in the HFE gene.
The LAMP Human Hemochromatosis KIT is an in vitro diagnostic test intended for the qualitative detection of the mutations C282Y (rs1800562) and H63D (rs1799945) on EDTA whole blood and extracted DNA.
The LAMP Human Hemochromatosis 3mut KIT is an in vitro diagnostic test intended for the qualitative detection of the mutations C282Y (rs1800562), H63D (rs1799945) and S65C (rs1800730) on EDTA whole blood and extracted DNA.
Genetic Thrombosis
Inherited thrombophilia is associated with an increased risk of venous thromboembolism. Genotyping supports risk assessment in recurrent thrombosis, family history, or before pregnancy, hormonal contraception or surgery.
LaCAR provides CE-IVD kits for these markers, run from the primary sample.
LaCAR provides CE-IVD kits for these markers, run from the primary sample.
Autoimmune Diseases
HLA-B27 is associated with the spondyloarthropathies, including ankylosing spondylitis and acute anterior uveitis. Typing contributes to the diagnostic work-up of patients with suggestive symptoms.
LaCAR offers CE-IVD HLA-B27 assays.
LaCAR offers CE-IVD HLA-B27 assays.
Food Intolerance
Genotyping identifies the genetic basis of primary lactose intolerance (lactase non-persistence) and the HLA-DQ2/DQ8 haplotypes associated with coeliac disease.
LaCAR provides CE-IVD kits for these markers, run from the primary sample.
LaCAR provides CE-IVD kits for these markers, run from the primary sample.
You have a question regarding our products ? You want to know more about our method ?
Find out about our other expertises
Genetic testing
CE Kits
Newborn Screening
Genetic testing
CE Kits
Pharmacogenetics
