The best way to be informed about your genetic profile and your genetic risking
Some of us harbor pathogenic mutations in the DNA, which are not manifest yet but may cause serious health problems in the future, from cancer to cardiac arrest. Furthermore, we all are healthy carriers of at least 1 to 8 genetic diseases, which we can pass on to affected offspring. Last, but not least, our individual reaction to certain drugs may be different.
Our Proactive testing is the real next generation of predictive genetic screening.
We are different because:
Cerebrovascular Diseases
Genetic Stroke Syndromes
Cardiovascular Disorders
Cardiac Arrhythmias
Sudden Death
Hereditary Breast and Ovarian cancer
Other Genetic Susceptibilities to Cancer
Connective Tissue Disorders
Storage Diseases and Metabolic Disorders
Myopathic and Neurological Conditions
[Screening of pathogenic mutations deposited in human databases]:
Congenital syndromes
Deafness
Vision Loss
Mental Retardation
Metabolic Disorders
Skeletal Dysplasias
Epilepsies
Others
[bioinformatic screening of new mutations, not deposited in human databases yet]:
Congenital syndromes
Mental Retardation
Metabolic Disorders
Skeletal Dysplasias
Vision Loss
Deafness
Epilepsies
Others
Alcohol tolerance
Caffeine tolerance
Bitter taste sensitivity
Other Nutrigenetics
Malignant Hyperthermia
Statin Sensitivity