![]() ![]() Faults in this gene can cause Duchenne muscular dystrophy (DMD), a serious congenital and gender related muscular disorder. Koen Devriendt, clinical geneticist at UZ Leuven. “We are the first centre in the world to also examine a specific gene, the DMD gene, in the mother’s DNA via a NIPT test,” explained Professor Dr. These tests were all included in a study into potentially relevant additional results. In the twelve month period following the introduction of reimbursement CME conducted a total of 26,123 NIPT analyses. The NIPT test has been reimbursed by health insurance funds in Belgium since 1 July 2017. This way not only can the three major, viable chromosomal abnormalities (trisomy 21, 18 and 13) be traced, but also other genetic defects in both the baby and the mother. All of them apply an extensive, genome wide version of the NIPT, which examines all DNA fragments in the sample. ![]() The Centre for Human Genetics (CME) is one of eight medical genetics centres in Belgium. The test is primarily intended to trace major chromosomal abnormalities in the baby’s DNA, because they can lead to serious disorders such as Down’s syndrome (trisomy 21). More than 80% of pregnant women now opt to give a blood sample and have a non-invasive prenatal test (NIPT). The blood of a pregnant woman contains not only her own DNA but also fragments of the baby’s genetic material. ![]()
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