Consciously plan your family from Gyncentrum

Plan your pregnancy, reducing the risk of transmitting a genetic disease to your child.

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When is it a good idea to do family planning genetic testing?

If you are planning a pregnancy and want to reduce the risk of transmitting a possible genetic disease to your child.

If you want to find out to what extent you are at risk of conceiving a child burdened with a genetic disease.

If you are experiencing habitual miscarriages of unexplained cause.

FAMILY PLANNING

Why Gyncentrum?

Gyncentrum the No. 1 center in Poland for family planning and infertility diagnosis

The Gyncentrum laboratory is one of the most modern laboratories in Europe. We have the largest offer of diagnostic tests for family planning and infertility on the Polish market. The team of the Gyncentrum Laboratory consists of high-class specialists in laboratory diagnostics, genetics and biotechnology. Patients perform genetic, cytogenetic and immunological tests with us.

Consciously plan your family.
Make an appointment for a genetic test at Gyncentrum.

+48 600 466 592

Learn about our genetic testing offerings

toward family planning

family planning

FertiSCREEN

The FertiSCREEN test is a unique opportunity to precisely test 129 selected genes associated with genetic diseases most common in the Polish population, i.e. cystic fibrosis, phenylketonuria, spinal muscular atrophy, Tay Sachs disease and others. The presence of a recessive mutation in the same genes in both partners poses as much as a 25% risk of giving birth to a sick child.

Important!

Carriers of diseases inherited in an autosomal recessive manner are healthy and are usually unaware of having a defective gene. For an autosomal recessively inherited disease to manifest, the mutation must affect both copies of the gene in question. This is why it is important for a couple planning a pregnancy to know whether they carry mutations in the same genes, which would carry a high risk of passing on the genetic disease to a future child.

family planning

WES DUO

Whole-exome sequencing – WES is the most extensive study of the coding parts of the genome available on the market today, in which up to 20,000 genes are analyzed. A change in any one of them can lead to the development of a genetic disease, such as those manifested by autism spectrum disorders.

In the case of WES DUO, whole exome analysis of prospective parents is performed using the NGS method. The sequenced genes are examined for the presence of carriers of all (the rare ones too) known autosomal recessively inherited diseases. At the same time, the risk of a given disease in the offspring is estimated.