Genetic Tests
Knowing Risk Factors
In human genetics, disease conditions encompass a variety of genetic disorders caused by anomalies or mutations in the human genome. These disorders can be inherited in various ways. One in seven individuals carries a genetic predisposition for rare diseases. Understanding one’s risk factors enables proactive measures to maintain health or delay and mitigate the onset of the disease.
At Hanse Genetik, we conduct various genetic tests to diagnose risk factors. Some of the diseases we can detect include:
Rare DiseasesPathology
- Neurogenetic diseases
- Epilepsy
- Parkinson’s Disease
- Dementia
- CADASIL
- Hereditary Tumor Diseases
- Breast and Ovarian Cancer
- Colorectal Cancer
- Hereditary Kidney Diseases
- Malignant Hyperthermia
- Hereditary Eye Diseases
- Retinitis Pigmentosa
- Optic Atrophy
- Hereditary Metabolic Diseases
- Thrombophilia
- Medication Use During Pregnancy
- Mitochondrial Diseases
- Genetically Caused Developmental Disorders
- Dysmorphic Syndromes
- Mental Retardation
- Hydrocephalus
- Trisonomy 21
- Wiedemann-Beckwith Syndrome
- Reproductive Genetics for Fertility
- Other genetically related conditions such as Cleft Lip, Cleft Palate.
To get an overview of our entire range of services, please select the respective category under Diagnostics.
Hanse Genetik is a member of the National Alliance for Rare Diseases (NASGE).
