GENICA offers genetic tests for close to 300 rare diseases
GENICA Lab offers genetic tests for close to 300 rare diseases. In the enclosed brochure you will find detailed information about the tests, the genes studied, and the fees.
Our list of genetic tests for rare decease is continuously updated. Contact us if you cannot find a specific test you need.
Diagnostic Range: Genetic tests for rare diseases
Diagnostic Methods: Sanger sequencing / MLPA/Fragment analysis
Results within: 10 business days
Fees: From BGN 40 to BGN 5000 depending on the test performed
Next-Generation sequencing (NGS)/ Whole Exome Sequencing (WES)
This test detects mutations in 20,000 genes associated with various hereditary conditions. It analyzes packages of target genes associated with specific conditions according to clinical diagnosis (Cancer Panel, Pediatric Panel, Diabetes Panel, Epilepsy Panel, Intellectual Deficiency/Autism Panel, Skeletal Dysplasias Panel, Cardiomyopathies Panel, etc.).
Diagnostic Range: ~20 000 genes
Diagnostic Method: Next-Generation Sequencing
Research Material: Venous blood
Results within: 2 to 4 months
Fee: BGN 3800
Cancer, childhood diseases, diabetes, epilepsy, intellectual deficit/autism, skeletal dysplasia, cardiomyopathies, etc.