Literature DB >> 12853237

Progressive supranuclear palsy phenotype secondary to CADASIL.

J A Van Gerpen1, J E Ahlskog, G W Petty.   

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.

Entities:  

Mesh:

Year:  2003        PMID: 12853237     DOI: 10.1016/s1353-8020(02)00146-3

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  6 in total

1.  Vascular parkinsonism in a CADASIL case with an intact nigrostriatal dopaminergic system.

Authors:  F Wegner; K Strecker; J Schwarz; A Wagner; W Heinritz; F Sommerer; D R Thal; J-P Schneider; K Kendziorra; O Sabri
Journal:  J Neurol       Date:  2007-11-21       Impact factor: 4.849

2.  First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family.

Authors:  Raffaella Valenti; Silvia Bianchi; Francesca Pescini; Camilla D'Eramo; Domenico Inzitari; Maria Teresa Dotti; Leonardo Pantoni
Journal:  J Neurol       Date:  2011-03-16       Impact factor: 4.849

Review 3.  Neuroimaging Pearls from the MDS Congress Video Challenge. Part 1: Genetic Disorders.

Authors:  Diana A Olszewska; Sapna Rawal; Conor Fearon; Paula Alcaide-Leon; Rick Stell; Vijayashankar Paramanandan; Tim Lynch; Tania Jawad; Padmaja Vittal; Brandon Barton; Hiroaki Miyajima; Satoshi Kono; Rukmini Mridula Kandadai; Rupam Borgohain; Anthony E Lang
Journal:  Mov Disord Clin Pract       Date:  2022-02-03

Review 4.  Neuropsychiatric manifestations in CADASIL.

Authors:  Hugues Chabriat; Marie-Germaine Bousser
Journal:  Dialogues Clin Neurosci       Date:  2007       Impact factor: 5.986

Review 5.  Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders.

Authors:  Sonja W Scholz; Jose Bras
Journal:  Int J Mol Sci       Date:  2015-10-16       Impact factor: 5.923

6.  Case Report: Progressive Asymmetric Parkinsonism Secondary to CADASIL Without Dementia.

Authors:  Weihang Guo; Baolei Xu; Hong Sun; Jinghong Ma; ShanShan Mei; Jingrong Zeng; Junyan Sun; Erhe Xu
Journal:  Front Neurol       Date:  2022-01-10       Impact factor: 4.003

  6 in total

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