Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2004-10-7
pubmed:abstractText
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.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1351-5101
pubmed:author
pubmed:issnType
Print
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
663-9
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:15469450-Adult, pubmed-meshheading:15469450-Alanine, pubmed-meshheading:15469450-Amyloid beta-Peptides, pubmed-meshheading:15469450-Brain, pubmed-meshheading:15469450-DNA Mutational Analysis, pubmed-meshheading:15469450-Dementia, pubmed-meshheading:15469450-Family Health, pubmed-meshheading:15469450-Female, pubmed-meshheading:15469450-Humans, pubmed-meshheading:15469450-Immunohistochemistry, pubmed-meshheading:15469450-Lewy Bodies, pubmed-meshheading:15469450-Magnetic Resonance Imaging, Cine, pubmed-meshheading:15469450-Membrane Proteins, pubmed-meshheading:15469450-Middle Aged, pubmed-meshheading:15469450-Mutation, Missense, pubmed-meshheading:15469450-Nerve Tissue Proteins, pubmed-meshheading:15469450-Neurofibrillary Tangles, pubmed-meshheading:15469450-Neuropsychological Tests, pubmed-meshheading:15469450-Parkinsonian Disorders, pubmed-meshheading:15469450-Peptide Fragments, pubmed-meshheading:15469450-Postmortem Changes, pubmed-meshheading:15469450-Presenilin-1, pubmed-meshheading:15469450-Synucleins, pubmed-meshheading:15469450-Valine
pubmed:year
2004
pubmed:articleTitle
New V272A presenilin 1 mutation with very early onset subcortical dementia and parkinsonism.
pubmed:affiliation
Hospital Ramon y Cajal, Universidad de Alcala, Madrid, Spain. adriano.jimenez@hrc.es
pubmed:publicationType
Journal Article, Comparative Study