Presence of gene mutations in both parents increases risk for disease in their children. PGS.carrier investigates such recessive genes including those causing Bloom syndrome, Gaucher disease, fructose intolerance, cystic fibrosis, MCAD-, and alpha-1-antitrypsin- deficiency. PGS.carrier also includes investigation of genes that increase risk for diseases and malformations in offspring (e.g. Crohn's disease and spina bifida).
The result informs you and your partner about the risk for a genetic disease in your offspring.