Genetic Study of Amyotrophic Lateral Sclerosis in Norway
ConditionAmyotrophic Lateral Sclerosis
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16-100
SponsorSykehuset Telemark
The purpose of this study is to explore the genetic causes relevant for ALS development in Norway.
Probable or definite ALS
Eligible to consent
None
Individuals diagnosed with ALS that are being followed through the Norwegian health-care system.
Case-only
Cross-sectional
Observation
Other interventionObservation of genetic characteristics
Gene frequency
Number of patients with disease causing mutations in high penetrant ALS genes
New ALS genes
Identify new ALS genes in the Norwegian ALS population
Genetic risk factors
Identify genetic risk factors for ALS in Norway.
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