In many families, severe neurological diseases are inherited – such as Parkinson's disease, ataxia or dystonia. These are diseases that can cause tremors, balance problems or involuntary movements. In many cases, similar problems run in the family, which suggests that it is hereditary. But despite advanced tests, healthcare cannot find an explanation.
Andreas Puschmann, professor of neurology at Lund University, explains how the research combines DNA analyses, medical examinations and family history to identify patterns that can explain the origin of the diseases. The goal is to give hope to families without a diagnosis – and to contribute to a deeper understanding of what actually controls how certain diseases arise and are passed on.
Organized in collaboration with Lund University and the Crafoord Foundation. Free entry, no pre-registration required.