For the screening of aneuploidies in Chromosome 21 only – able to determine fetal sex.
For the screening of aneuploidies in Chromosomes – 13,18,21, X and Y – able to determine fetal sex. The most common chromosomal aneuploidies detected are:-
Trisomy 21 – Downs Syndrome
Trisomy 18 – Edwards Syndrome
Trisomy 13 – Patau Syndrome
Monsomy X – Turner Syndrome
XXX – Trisomy X
XXY – Klinefelter Syndrome
XYY – Jacobs Syndrome.
|£375 (£399 including scan)|
This test screens for the five most common inherited recessive genetic disorders such as Cystic Fibrosis, Beta Thalassemia, Sickle cell Anaemia and Deafness Autosomal recessive type 1a and 1b.
|Genesafe De Novo|
This test screens for 44 severe genetic disorders as a result of de novo mutations (a gene mutation that is not inherited) in 25 genes.
Analyses every chromosome in the genome providing karyotype-level insight. Tests for the most common aneuploidies as in Ninalia 5 but includes the less frequent chromosomal aneuploidies in Trisomy 1-22.
|£800 – including scan|
The most comprehensive NIPT in the world which analyses every chromosome in the genome as well as 9 clinically significant microdeletion syndromes which are:-
1p36 deletion Syndrome.
|£1000 – including scan|
This test screens for both the inherited and de novo single-gene disorders with the combined test providing a complete picture of any potential risk to the pregnancy.
is a combination of the two most powerful tests available worldwide PrenatalSafe KaryoPlus + GeneSafe complete are offered together at a reduced price.