Bardet-Biedl Syndrome
Leber congenital Amaurosis – Panel
Warburg Micro Syndrome
SOD2 (MnSOD) – Polymorphisms
CardioNext
CardioNext® is a genetic test for the analysis of polymorphisms associated with an increased risk of onset of cardiovascular diseases. The aim of the test is to determine individual risk profiles for personalized treatments and early prevention of these diseases. The onset of cardiovascular diseases is induced by various factors such as diet and lifestyle […]
CardioScreen® Cardiomiopathy
CardioScreen-Cardiomiopatie® is a diagnostic test that allows you to perform a multiple genetic analysis to assess the presence of mutations associated with inherited cardiomyopathies. The test identifies patients at risk for potentially fatal cardiac events, through the analysis of their DNA.
Lactic Acidosis and Piruvate Metabolism – Panel
Albinism Oculocutaneous – Panel
Retinitis Pigmentosa – Reduced Panel
AutismScreen®
AutismScreen™ is the non-invasive genetic test that screens for autism spectrum disorders in children. The diagnosis of Autism Spectrum Syndromes is not simple and is made only on the basis of behavioral indicators. The AutismScreen ™ test can be a valuable aid for the early identification of a mutation related to a disease. The AutismScreen […]
