Article
CSF studies facilitate DNA diagnosis in familial Alzheimer's disease due to a presenilin-1 mutation.
Journal of Alzheimer's disease : JAD - 1 Jan 2009
de Bot Susanne T, Kremer H P H, Dooijes Dennis, Verbeek Marcel M
Abstract excerpt
In sporadic Alzheimer's disease (AD), cerebrospinal fluid (CSF) analysis is becoming increasingly relevant to establish an early diagnosis. We present a case of familial AD due to a presenilin-1 mutation in which CSF studies suggested appropriate DNA diagnostics. A 38 year old Dutch man presented with dementia, spastic paraparesis, and frontal executive function impairments, mimicking familial Creutzfeldt Jakob...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
