GENETIC TESTING/

PROACTIVE

Be informed, be healthy, be protected

Be Proactive about your health.

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.

From the Experts in Rare Diseases,
the Screening for Healthy Individuals

Our Proactive testing is the real next generation of predictive genetic screening.

We are different because:

We come from the clinical experience

We always do the full sequence

We analyse the results manually

How does Proactive help you?

You can

How does Proactive help you?

You can

Which conditions do you screen for?

Actionable Genetic Diseases

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

Hereditary Transmissible Diseases (1st Level)
Recessive genetic disorders which can be passed on to affected offspring

[Screening of pathogenic mutations deposited in human databases]:

Congenital syndromes

Deafness

Vision Loss

Mental Retardation

Metabolic Disorders

Skeletal Dysplasias

Epilepsies

Others

Hereditary Transmissible Diseases (2nd Level)
Recessive genetic disorders which can be passed on to affected offspring

[bioinformatic screening of new mutations, not deposited in human databases yet]:

Congenital syndromes

Mental Retardation

Metabolic Disorders

Skeletal Dysplasias

Vision Loss

Deafness

Epilepsies

Others

Nutrigenetics

Alcohol tolerance

Caffeine tolerance

Bitter taste sensitivity

Other Nutrigenetics

 

Pharmacogenomics (1st Level)

Malignant Hyperthermia

Statin Sensitivity

Pharmacogenomics (2nd Level)

Group 1A variants from the PharmGKB database, with clinical administration guidelines or FDA-approved drug label annotation.

Which conditions do you screen for?

Actionable Genetic Diseases

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

Hereditary Transmissible Diseases (1st Level)
Recessive genetic disorders which can be passed on to affected offspring
[Screening of pathogenic mutations deposited in human databases]:

Congenital syndromes

Deafness

Vision Loss

Mental Retardation

Metabolic Disorders

Skeletal Dysplasias

Epilepsies

Others

Hereditary Transmissible Diseases (2nd Level)
Recessive genetic disorders which can be passed on to affected offspring
[bioinformatic screening of new mutations, not deposited in human databases yet]:

Congenital syndromes

Mental Retardation

Metabolic Disorders

Skeletal Dysplasias

Vision Loss

Deafness

Epilepsies

Nutrigenetics

Alcohol tolerance

Caffeine tolerance

Bitter taste sensitivity

Other Nutrigenetics

 

Pharmacogenomics (1st Level)

Malignant Hyperthermia

Statin Sensitivity

Pharmacogenomics (2nd Level)

Group 1A variants from the PharmGKB database, with clinical administration guidelines or FDA-approved drug label annotation.

Which conditions do you screen for?

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

Recessive genetic disorders which can be passed on to affected offspring

[Screening of pathogenic mutations deposited in human databases]:

Congenital syndromes

Deafness

Vision Loss

Mental Retardation

Metabolic Disorders

Skeletal Dysplasias

Epil