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Eur J Neurol ; 10(3): 319-23, 2003 May.
Article in English | MEDLINE | ID: mdl-12752408

ABSTRACT

The clinical, neuropsychological and neuropathological features of a patient with early-onset Alzheimer's disease as a result of the M139V presenilin-1 (PSEN-1) mutation are presented, and compared with previous reports of patients with the same mutation. Similarities, such as the age at onset and the relative preservation of naming skills, and differences, such as the significant basal ganglia, thalamic and cerebellar pathology, are noted. This clinical and pathological heterogeneity in patients with the same PSEN-1 mutation suggests phenotype modulation by genetic and/or epigenetic factors.


Subject(s)
Alzheimer Disease/genetics , Alzheimer Disease/physiopathology , Membrane Proteins/genetics , Mutation , Cerebellar Cortex/metabolism , Cerebellar Cortex/pathology , Cerebral Cortex/metabolism , Cerebral Cortex/pathology , Humans , Male , Methionine/genetics , Middle Aged , Phenotype , Presenilin-1 , Thalamus/metabolism , Thalamus/pathology , Valine/genetics
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