PSP-Richardson's Syndrome as a Rare Phenotypic Expression of Very Late-Onset Huntington's Disease: A Case Report
Mov Disord Clin Pract
.
2024 Mar;11(3):303-305.
doi: 10.1002/mdc3.13943.
Epub 2024 Jan 3.
Authors
Stephane Prange
1
2
3
,
Chloé Laurencin
1
,
Pauline Roche
1
,
Isabelle Quadrio
4
,
Stéphane Thobois
1
2
3
Affiliations
1
Hospices Civils de Lyon, Department of Neurology C, Expert Parkinson Center NS-PARK/FCRIN, Pierre Wertheimer Neurological Hospital, Bron, France.
2
Univ Lyon, Marc Jeannerod Cognitive Neuroscience Institute, CNRS, UMR 5229, Bron, France.
3
Univ Lyon, Faculté de Médecine et de Maïeutique Lyon Sud Charles Mérieux, Université Claude Bernard Lyon 1, Oullins, France.
4
Hospices Civils de Lyon, Neurobiology and Neurogenetics, Department of Biochemistry and Molecular Biology, Lyon, France.
PMID:
38173343
PMCID:
PMC10928328
DOI:
10.1002/mdc3.13943
No abstract available
Keywords:
Huntington's disease; Richardson's syndrome; progressive supranuclear palsy.
Publication types
Case Reports
Letter
MeSH terms
Humans
Huntington Disease* / diagnosis
Phenotype
Supranuclear Palsy, Progressive* / metabolism