Monday-Sunday 08:30 - 20:00
г. Киев, ул. Ковпака 17 (On the map)
г. Белая Церковь, ул. Таращанская 191А (On the map)
Geneticist in Kyiv: consultations for children and adults on hereditary and congenital conditions. A geneticist consultation in Kyiv can help identify risks in time and obtain an accurate diagnosis and recommendations. A pediatric geneticist with a modern approach and individual follow-up sees patients at the center.
A geneticist in Kyiv is involved when the clinical picture does not fit standard pediatric or neurological protocols. At CSM Clinic in Kyiv, we work within evidence-based medical genetics and focus not only on confirming a diagnosis but also on building a clear strategy of next steps for the care of the adult or child.
The first visit includes a structured collection of family history and an analysis of the course of pregnancy. The geneticist in Kyiv assesses the phenotypic features of the adult or child and creates an individual diagnostic plan.
Interpreting the results is a mandatory step. Genetic counseling includes explaining the findings and discussing:
The range of conditions the doctor works with is very broad:
Quality diagnosis requires teamwork. CSM Clinic in Kyiv provides a multidisciplinary approach in which the geneticist works side by side with other experts. If a genetic cause of developmental disorders is confirmed or ruled out, related specialists join the work for comprehensive rehabilitation:
It is worth seeing a geneticist in Kyiv when planning a pregnancy, in cases of infertility or recurrent pregnancy loss, if there are hereditary diseases in the family, or if a child is suspected of having developmental delay.
A geneticist diagnoses chromosomal abnormalities, monogenic diseases, and metabolic disorders, and also assesses genetic predisposition to cancer.
At the appointment, the geneticist draws up the family tree, examines for external signs of genetic disorders, and estimates the risks of inheriting diseases.
The main tests include karyotyping to assess chromosomes, DNA tests for mutations, genetic panel screenings, and noninvasive prenatal tests.
When planning a pregnancy, karyotyping of both partners, carrier screening for spinal muscular atrophy (SMA) and cystic fibrosis, and a check of the folate cycle are recommended.
