An advanced carrier screening test that, using next-generation DNA sequencing techniques, allows us to identify couples at risk of transmitting the most common genetic diseases to their children, identifying DNA mutations of which one or both parents may be unaware carriers.
CARRIERADVANCE Focus – Panel for the COUPLE
Genes analyzed: 30
Genetic diseases investigated: 31 of the most common in the Italian population, including Cystic Fibrosis, Beta Thalassemia, Sickle Cell Anemia and Hereditary Deafness (Type 1A and 1B), Muscular Atrophy (SMA 1) etc.
With this booking the test is performed on both partners.
Preparation for the exam
- No preparation is required for the exam.
- It is not necessary to fast.
Result ready in 20-30 working days, also by email.
The test can be done by taking a blood sample or a buccal swab.
ATTENTION: the exam is NOT performed on patients under 10 years of age
For genetic analysis the cost of the sample is €15.00.
(If you have a doctor's recommendation, please bring it to the time of the examination)
