Blood

Molecular karyotype by aCGH is an advanced genetic test thatóry identifies uncompensated chromosomal abnormalities associated with birth defects. It utilizes a porónary genomic hybridization with microarray (aCGH) method for accurate karyotype analysis.

The genetic test involves the analysis of 67 cancer-related genes and assesses the risk of rós different typesóof cancer in a single test.

The blood test is based on the measurement of malondialdehyde levels, an indicator of oxidative stress thatós increased in cardiovascular, nervous system, metabolic and cancer diseases.

The test detects the presence of genetic material (RNA) of the hepatitis D virus (HDV), the causative agent of viral hepatitis.

The test detects the presence of genetic material (RNA) of hepatitis G virus (HGV), the causative agent of viral hepatitis.

The test involves the determination of the compound fibronectin, a glycoprotein involved in ra

The blood test measures the level of the enzyme acid alpha-glucosidase, whose deficiencyór is associated with Pompe disease (glycogenosis type II), a genetically determined storage disease.

The test allows the detection of macroamylase, amylase enzyme complexesós and immunoglobulins for the diagnostic rós of acute pancreatitis and other conditionsów.

A blood test that measures amitriptyline levels, used in monitoring antidepressant therapy.

A blood test that measures mitotane levels, used in monitoring cancer therapy.