Pre-eclampsia is a syndrome which can present from 20 weeks of pregnancy, probably due to an alteration in the maternal uteroplacental blood flow. This is one of the main causes of maternal and perinatal morbidity and mortality. Early detection of pre-eclampsia is key for the survival of the mother and the foetus. Pre-eclampsia is a serious complication which occurs in 3-5% of pregnancies. Sometimes pre-eclampsia does not cause symptoms, high blood pressure can appear suddenly or slowly. Women with chronic hypertension and existing conditions before pregnancy require special medical supervision and follow-up.

BBsafe allows the presence of genomic sequences from the foetus and present in maternal blood to be studied and thus the level of risk for the corresponding syndrome to be determined. BBsafe tests are carried out by the Analiza Group laboratory in Spain.

STANDARD BBSAFE 

Trisomy 21 (Down’s Syndrome) Trisomy 18 (Edwards’ Syndrome) Trisomy 13 (Patau’s Syndrome) Sex chromosome aneuploidies (Turner syndrome, Klinefelter syndrome, XYY syndrome ...). Foetal sexing (for patients who choose this).

BBsafe allows the presence of genomic sequences from the foetus and present in maternal blood to be studied and thus the level of risk for the corresponding syndrome to be determined. BBsafe tests are carried out by the Analiza Group laboratory in Spain.

BBSAFE ADVANCE

Trisomy 21 (Down’s Syndrome) Trisomy 18 (Edwards’ Syndrome) Trisomy 13 (Patau’s Syndrome) Sex chromosome aneuploidies (Turner syndrome, Klinefelter syndrome, XYY syndrome ...). Foetal sexing (for patients who choose this); the 7 most common microdeletion Syndromes. In addition, all chromosomes are analysed, providing the most information possible to date from non-invasive prenatal tests.

BBsafe allows the presence of genomic sequences from the foetus and present in maternal blood to be studied and thus the level of risk for the corresponding syndrome to be determined. BBsafe tests are carried out by the Analiza Group laboratory in Spain.

BBSAFE PLUS 

Trisomy 21 (Down’s Syndrome) Trisomy 18 (Edwards’ Syndrome) Trisomy 13 (Patau’s Syndrome) Sex chromosome aneuploidies (Turner syndrome, Klinefelter syndrome, XYY syndrome ...). Foetal sexing (for patients who choose this); the 3 most common microdeletion Syndromes.