Specific genetic tests

Cydrug	Analysis of genetic variations linked to the elimination of a specific medication. This analysis allows the calculation of the correct dosage, to reduce side effects and the use of ineffective medicines.
Antitryps	Looks for gene-type α-1-antitrypsine, which is an indicator in the diagnosis of emphysema or chronic obstructive respiratory problems.
Thalass	Analysis recommended when there is a suspicion of β-thalassemia in patients from the Mediterranean area, when a parent is a known carrier (hetero or homozygote) of one or several mutations of β-globin gene.
HLA B27	Genetic research of HLA B27 allele is recommended when there is a suspicion of ankylosing spondylitis, spondylarthropathies following bacterial or viral infections, reactive arthritis, psoriasis arthritis, Behcet syndrome, acute anterior uveitis, chronic juvenile arthritis, Whipple disease, Crohn’s disease, ulcerated colitis and Reiter syndrome. This molecular approach must, however, be carried out in conjunction with other clinical and radiological examinations.