Progressive supranuclear palsy phenotype secondary to CADASIL

Parkinsonism Relat Disord. 2003 Aug;9(6):367-9. doi: 10.1016/s1353-8020(02)00146-3.

Abstract

Background and purpose: To report a unique case of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy manifesting as a progressive supranuclear palsy phenotype, thereby expanding its recognized presentations.

Methods: Review of the pertinent literature from MEDLINE, cross-referencing cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, progressive supranuclear palsy, and parkinsonism. Description of a 60-year-old woman who presented with a several year history of step-wise, progressive parkinsonism secondary to cerebral autosomal dominant arteriopathy.

Results: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy may present with a progressive supranuclear phenotype.

Conclusion: Parkinsonism, including a progressive supranuclear palsy phenotype, is one of a growing number of recognized ways that cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy may present.

Publication types

  • Case Reports

MeSH terms

  • Dementia, Multi-Infarct / complications
  • Dementia, Multi-Infarct / diagnosis*
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Middle Aged
  • Supranuclear Palsy, Progressive / etiology*
  • Syndrome