Cardiovascular  Hereditary syndromes (Risk assessment)   FAMILION®: HCM

FAMILION®: HCM 

Test
  FAMILION®: HCM 
Related to
  Hereditary hypertrophic cardiomyopathy (pathological thickening of the cardiac muscle)
Target population
  Individuals suspected as suffering from hereditary pathological thickening of the cardiac muscle, based on suspicious ECHO findings, unexplained events of loss of consciousness, or family members with diagnosed disease.
Objective
  To establish a diagnosis of hypertrophic cardiomyopathy in order to tailor follow-up and treatment, to prevent future events of loss of consciousness and sudden death
Sample type
  Peripheral blood
Procedure
  Genetic diagnosis of blood cells
Availability