Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: A novel entity?

Klas Wictorin, Björn Brådvik, Karin Nilsson, Maria Soller, Danielle van Westen, Gunnel Bynke, Peter Bauer, Ludger Schöls, Andreas Puschmann

Research output: Contribution to journalArticlepeer-review

3 Citations (SciVal)
206 Downloads (Pure)

Abstract

We describe the clinical characteristics of a Swedish family with autosomal dominant cerebellar ataxia, sensory and autonomic neuropathy, additional neurological features and unknown genetic cause.
Original languageEnglish
Pages (from-to)748-754
JournalParkinsonism & Related Disorders
Volume20
Issue number7
DOIs
Publication statusPublished - 2014

Bibliographical note

The information about affiliations in this record was updated in December 2015.
The record was previously connected to the following departments: Neurology, Lund (013027000), Ophthalmology (Lund) (013043000), Diagnostic Radiology, (Lund) (013038000), Division of Clinical Genetics (013022003), Department of Psychogeriatrics (013304000)

Subject classification (UKÄ)

  • Neurology

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