Early and severe autonomic failure: broadening the clinical phenotype of type-2 spinocerebellar ataxia. A case report

J Neurol. 2015 Jan;262(1):224-5. doi: 10.1007/s00415-014-7577-3. Epub 2014 Nov 20.

Authors

R Capozzo¹, G Rizzo, M De Mari, C Tortorella, G Logroscino

Affiliation

¹ Neurodegenerative Diseases Unit, Department of Clinical Research in Neurology, University of Bari at Pia Fondazione Card G. Panico Hospital, Via San Pio n. 4, 73039, Tricase (LE), Italy.

PMID: 25408369
DOI: 10.1007/s00415-014-7577-3

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Humans
Male
Phenotype
Pure Autonomic Failure / etiology
Pure Autonomic Failure / physiopathology*
Spinocerebellar Ataxias / complications
Spinocerebellar Ataxias / genetics
Spinocerebellar Ataxias / physiopathology*