Genetic Diseases / Syndromes Testing

Technological developments in molecular genetics have allowed us the rapid application of methods for the reliable detection of any known mutations that lead to the development of genetic syndromes and diseases such as Thalassemia, Cystic Fibrosis, neuromuscular diseases, etc.

Access To Genome laboratories have the necessary equipment, know-how and experience for the reliable application of these methods to enable the diagnosis of even very rare genetic diseases and syndromes in cases with clinical manifestations, family history or other relevant indications while it is possible to create a control panel of multiple genes simultaneously using the Next Generation Sequencing – NGS.