Genomics Services
 
 
Lactose Intolerance
Lactose intolerance is a genetic gastrointestinal disorder in which body is unable to digest lactose – a sugar found in milk and dairy products. Medically this condition is called Hypolactasia. Ingestion of milk may lead to abdominal cramps, bloating, distension, flatulence and diarrhea. Symptoms of lactose intolerance are sometimes intolerable by patient. Mutation in MCM6 gene is responsible for fluctuation in production of lactase enzyme in humans. This condition is inherited in autosomal recessive pattern, where the parents which carries faulty gene have chances to pass this gene to their children.

Sample Type

Saliva Sample: Min 2ml Saliva Sample or blood in pre-designed kits provided by Xcelris Labs.
 
Brochure           inquiry
 
 
Beta Thalassemia   |   Sickle Cell Anemia   |   MTHFR (Methylenetetrahydrofolate reductase)
Lactose Intolerance   |   Cystic Fibrosis (CFTR Mutation)
Biotinidase Deficiency   |   Hereditary Hemochromatosis
 
 
Click Here to Zoom
 
Click Here to Zoom
 
Click Here to Zoom
 
Click Here to Zoom