Between the 11+1 and 13+6 week of gestation, a special ultrasound examination can be conducted at your request for early organ diagnosis, nuchal translucency measurement and, if applicable, in combination with blood examinations. After all results are available, the probability of a risk of trisomy of the chromosomes 13, 18 and 21 can be calculated and early organ malformations can be mostly excluded. To securely exclude a chromosomal disorder, genetic diagnosis of the child's cells may be conducted as well (e.g. non-invasive prenatal diagnostics = NIPT). We will gladly advise you about this as well.
The first-trimester screening is a self-payer service that unfortunately will not be reimbursed by the health insurances.