Format

Send to

Choose Destination
See comment in PubMed Commons below
Neurologia. 2010 Jan-Feb;25(1):13-6.

[New mutation in the PSEN1 (E120G) gene associated with early onset Alzheimer's disease].

[Article in Spanish]

Author information

  • 1Unitat d'Alzheimer i altres trastorns cognitius, Servei de Neurologia, ICN, Hospital Clínic de Barcelona, Institut d'Investigació Biomédica August Pi i Sunyer (IDIBAPS), Barcelona, España. allado@clinic.ub.es

Abstract

OBJECTIVE:

To describe a novel mutation in exon 5 of the presenilin 1 gene (E120G)associated with early-onset autosomal dominant Alzheimer's disease (AD).

PATIENT AND METHODS:

The proband was a man who began with memory loss and progressive cognitive decline at the age of 34. His father and his sister suffered from early-onset cognitive decline. The genetic study performed on the blood sample using the single strand conformation polymorphism (SSCP) technique did not detect any abnormality suggestive of the presence of a mutation in PSEN1, PSEN2, and APP. In the last stage of the disease the patient had seizures and gait alteration. He died at the age of 44. Coding exons 3-12 of PSEN1 were studied by direct sequencing using isolated DNA from frozen brain tissue of the proband.

RESULTS:

The neuropathological examination showed the presence of frequent amyloid plaques and neurofibrillary tangles and severe amyloid angiopathy. The direct sequencing of the PSEN1 gene disclosed the presence of the E120G mutation.

CONCLUSIONS:

E120G is a novel mutation in PSEN1 that probably causes early-onset autosomal dominant AD. Absence of genetic alterations in screening techniques (SSCP) does not rule out the presence of mutations. We recommend direct sequencing for the genetic study of patients with early-onset autosomal dominant AD.

PMID:
20388456
[PubMed - indexed for MEDLINE]
Free full text
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Ediciones Doyma, S.L.
    Loading ...
    Write to the Help Desk