Timely detection and diagnosis of heart disorders can lead to enhanced treatment options and improve prognosis. Having identified genetic variants associated with cardiology diseases in over 200 different genes, we can support you in providing your patients with a precise diagnosis of a cardiovascular disease. Testing can also identify asymptomatic and at-risk family members, facilitating precautions or interventions to prevent illness or sudden death.
Articles on Cardiovascular
Fabry disease (FD) is a rare lysosomal storage disorder also affecting the heart. Continuous cTNI elevation seems to occur in a substantial proportion of patients with FD.
Lessons from Everyday Stroke Care for Clinical Research and Vice Versa: Comparison of a Comprehensive and a Research Population of Young Stroke Patients
The comparison of baseline characteristics between the sifap1 study and the GQH registry revealed differences mainly determined by age.
Fabry disease (FD) is an X-linked inherited disease based on the absence or reduction of lysosomal-galactosidase (Gla) activity. The enzymatic defect results in progressive impairment of cerebrovascular, renal and cardiac function. Normally, female heterozygote mutation carriers are less strongly…
Pompe disease is a rare (estimated at 1 in every 40,000 births), inherited, and often fatal disorder that disables the heart and muscles. The goal of this study is to identify and validate a new biochemical marker from the plasma of affected patients helping to benefit other patients by an early…