Premium
New V272A presenilin 1 mutation with very early onset subcortical dementia and parkinsonism
Author(s) -
JimenezEscrig A.,
Rabano A.,
Guerrero C.,
Simon J.,
Barquero M. S.,
Güell I.,
Ginestal R. C.,
Montero T.,
Orensanz L.
Publication year - 2004
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/j.1468-1331.2004.00865.x
Subject(s) - medicine , dementia , parkinsonism , presenilin , psen1 , pathology , proband , dementia with lewy bodies , frontotemporal dementia , neuroscience , disease , alzheimer's disease , psychiatry , psychology , mutation , genetics , biology , gene
In this report, we present the clinical and pathological details of a kindred of four individuals with a novel missense mutation (V272A) of the presenilin 1 gene (PSEN1) that experienced a subcortical dementia. The age of onset of symptoms ranged 26–36‐year old, with an age at death of 36–46 years. Initial symptom was a marked mood disorder, with prominent parkinsonism in one case. The neuropsychological study, as well as the neuroimaging and PET in the proband were concordant with a subcortical dementia. The cerebral pathology showed in this patient, aside from the classical lesions of Alzheimer disease, Lewy bodies in cortex and substantia nigra, and widespread subcortical neuritic lesions. This clinical pattern and pathology expands the clinical spectrum of familial Alzheimer's disease and compel to include mutations of PSEN1 gene in the genetic study of subcortical dementia.