Morbus Fabry and Parkinson's Disease-More Evidence for a Possible Genetic Link

Susanne Müller; Jan Kassubek; Stephan T Hold; David C Kasper; Benjamin Mayer; Kathrin Müller; Axel Freischmidt; Reiner Siebert; Heiko Braak; Albert C Ludolph; Kelly Del Tredici

doi:10.1002/mds.29686

Morbus Fabry and Parkinson's Disease-More Evidence for a Possible Genetic Link

Mov Disord. 2024 Feb;39(2):449-451. doi: 10.1002/mds.29686. Epub 2024 Jan 16.

Authors

Susanne Müller¹, Jan Kassubek^{1

2}, Stephan T Hold³, David C Kasper³, Benjamin Mayer⁴, Kathrin Müller^{1

5}, Axel Freischmidt^{1

5}, Reiner Siebert⁵, Heiko Braak⁶, Albert C Ludolph^{1

2}, Kelly Del Tredici⁶

Affiliations

¹ Department of Neurology, University of Ulm, Ulm, Germany.
² German Center for Neurodegenerative Diseases (DZNE), Ulm, Germany.
³ ARCHIMED Life Science GmbH, Vienna, Austria.
⁴ Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany.
⁵ Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.
⁶ Clinical Neuroanatomy Section, Department of Neurology, Center for Biomedical Research, University of Ulm, Ulm, Germany.

PMID: 38226450
DOI: 10.1002/mds.29686

No abstract available

Keywords: Fabry's disease; GLA deficiency; Parkinson's disease; angiokeratoma diffuse; glycosphingolipids; α-galactosidase a (GLA) deficiency; α-galactosidase a (aGal).

Publication types

Letter

MeSH terms

Fabry Disease* / genetics
Humans
Mutation
Parkinson Disease* / genetics