Non-Invasive Prenatal Screening
NIPT (Non-Invasive Prenatal Screening)
Comprehensive prenatal screening for common chromosomal abnormalities from a single tube of maternal blood, starting from the 10th week of pregnancy.
ECEGEN Genetic Services
Our Services
Comprehensive genetic testing and counseling services from preconception onwards for the diagnosis and prevention of hereditary diseases.
Clinical Service
Medication in Pregnancy & Teratology Consultation
Personalized expert evaluation of medications and environmental factors encountered before or during pregnancy.
Consanguinity Risk Analysis
Consanguineous Marriage & Genetic Diseases
Risk of congenital anomalies in consanguineous marriages and preventive steps through genetic counseling.
IVF & Embryo Genetics
Preimplantation Genetic Diagnosis (PGD)
Selection of healthy embryos through genetic testing during IVF.
Preconception Screening
Preconception Carrier Screening
Carrier screening options tailored to couples based on family history and clinical assessment.
Patient & Family Counseling
Genetic Counseling
Expert genetic counseling for individuals at risk of hereditary diseases and carrier status.
Hereditary Oncology & Predisposition
Cancer Genetics and Hereditary Cancers
We assess hereditary cancer risk and analyze the tumor's genetic profile to help identify targeted drugs and treatment options.
BRCA1 / BRCA2 Screening
Hereditary Breast/Ovarian Cancer Genetic Testing
Determining hereditary breast and ovarian cancer risk through BRCA1/BRCA2 gene analysis.
Next-Generation Sequencing (NGS)
Clinical Exome and NGS Panels
Comprehensive variant analysis with clinical exome, whole genome sequencing, and disease-specific NGS panels.
Early Diagnosis & Carrier Testing
SMA Early Diagnosis & Carrier Test
Early diagnosis and carrier screening for SMA, a condition affecting motor neurons in the spinal cord.
DNA & Mutation Analysis
FMF / MEFV Genetic Testing
MEFV testing for familial Mediterranean fever, interpreted alongside clinical findings.
Clinical Examination & Pre-Diagnosis
Clinical Genetics
Detailed medical history, pedigree analysis, and dysmorphological examination by a Medical Genetics specialist.
DNA & Mutation Analysis
Molecular Genetics
Mutation and genotype analysis in single-gene, multifactorial, and mitochondrial disorders.
Karyotype Chromosome Analysis
Cytogenetics
Karyotyping service for numeric and structural chromosomal evaluation.
FISH & aCGH Methods
Molecular Cytogenetics
Detection of microdeletions and translocations using FISH, aCGH, and NGS methods.
RT-PCR Kit Development
Biotechnology
Biotechnological product and service work, including the development of RT-PCR diagnostic kits.
96 genes
Hereditary Cancer Panel
Multigene assessment of family history and hereditary cancer predisposition.
BRCA1BRCA2APCTP53PALB2
30 genes
Somatic Cancer and Biomarkers
Tumor-specific alterations and biomarker analyses supporting targeted therapy assessment.
EGFRKRASBRAFPIK3CATP53
53 genes
Colorectal Cancer Panel
Focused analysis of hereditary and somatic alterations associated with colorectal cancer.
APCKRASNRASBRAFMLH1
36 genes
Lung Cancer Panel
Comprehensive gene panel supporting diagnostic and treatment assessment in lung cancer.
EGFRALKROS1KRASMET
Targeted
Pancreatic Cancer Analyses
Hereditary risk genes and targeted molecular analyses associated with pancreatic cancer.
KRASBRCA1BRCA2PALB2ATM
36+ genes
Breast and Ovarian Cancer Panel
Genetic assessment of breast and ovarian cancer predisposition and tumor-specific alterations.
BRCA1BRCA2PALB2CHEK2PIK3CA