Article

Parkinsonism is a new pattern onset of CADASIL patients carrying with R544C Mutation: a case report

2023-03-21

Abstract excerpt

<h4>Background: </h4> Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant hereditary disease of cerebral small vessels. It is the most frequent heritable disease that causes stroke and vascular dementia. In China, patients carrying c.1630C>T (p.Arg544Cys) accounted for large proportion, typical symptoms including migraine with aura, transien...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 1bf297d9-b25b-5fca-a211-2c3452f06791
DOI: 10.21203/rs.3.rs-2679681/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Parkinsonism is a new pattern onset of CADASIL patients carrying with R544C Mutation: a case reportDOI 10.21203/rs.3.rs-2679681/v1Read

Short-term frequently relapsing ischemic strokes followed by rapidly progressive dementia in CADASIL: a case report and literature reviewSemantic proximity Read

[CADASIL with clinical manifestations of baldness, lumbago and Parkinson's symptoms].Semantic proximity Read

Clinical and Genetic Aspects of CADASILSemantic proximity Read

[Diagnosis, pathomechanism and treatment of CADASIL].Semantic proximity Read

Sex Differences in the Clinical and Imaging Characteristics of Korean CADASIL Patients: A Korean Nationwide Retrospective StudySemantic proximity Read

R558C NOTCH3 Mutation in a CADASIL Patient with Intracerebral Hemorrhage: A Case Report with Literature Review.Semantic proximity Read

Parkinsonism is a late, not rare, feature of CADASIL: a study on Italian patients carrying the R1006C mutation.Semantic proximity Read

Genotypic and phenotypic spectrum of CADASIL in Japan: the experience at a referral center in Kumamoto University from 1997 to 2014.Semantic proximity Read

Novel mutation of NOTCH3 gene in a Chinese Patient with CADASIL: A case reportSemantic proximity Read

A Chinese CADASIL family with p.R578C mutation at exon 11 of the NOTCH3 gene.Semantic proximity Read

Initially with pure parkinsonian phenotype of spinocerebellar ataxia type 3: A rare case report and literature reviewSemantic proximity Read

[CADASIL].Semantic proximity Read