Genetic researches
Genetic research can detect various genetic and chromosomal diseases. In certain cases, only genetic diagnosis makes it possible to establish a diagnosis and choose the correct medical tactics. The study of genetic information embedded in the DNA of a particular person helps to determinate many diseases or predisposition to them.
General genetic studies
- Karyotype (chromosomal analysis)
- Fragile X Chromosome (must be ordered with Chromosome Microarray Analysis)
- Chromosomal microarray analysis (if necessary with Fluorescent in situ hybridization (FISH))
- Fragile X Chromosome (must be ordered with Chromosome Microarray Analysis)
- Non-invasive prenatal examination "Invitae" (NIPS) – Aneuploidy + Microdeletions
- Invitae Core Carrier Screen (only CFTR, SMN1, FMR1) – Aneuploidy + Microdeletions
- Extensive Invitae Core Carrier research and Comprehensive gene carrier research
- Preimplantation Genetic Testing (PGT) (includes PGS/PGT-A and PGT-SR)
- Pregnancy loss analysis (also named products of conception (POC) analysis)
- Chromosomal microarray analysis of pregnancy loss
Genetic analysis differs from other types of diagnostics in the maximum accuracy of obtained results
Prenatal diagnosis (CVS/amniocentesis)
- Prenatal chromosomal microarray analysis (if necessary with Fluorescent in situ hybridization (FISH))
- Пренатальна інтерфазна флуоресцентна гібридизація in situ (FISH) (для 13, 18, 21, X, Y) (необхідно замовляти разом з каріотипом або мікроматрічним аналізом)
- Karyotype (chromosomal analysis)
- Amniotic fluid alpha-fetoprotein (AFP)
- AChE
Parental research and confirmation
- The test was carried out
- Fluorescence in situ hybridization for confirmation**
- Chromosome microarray analysis of parents
- Fluorescence in situ hybridization of parents
- Karyotype of parents (chromosomal analysis)
- Maternal Cell Contamination (MCC) Study
Get diagnosed or treated in a clinic
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