Literature DB >> 30838239

Corticobasal Syndrome in a Family with Early-Onset Alzheimer's Disease Linked to a Presenilin-1 Gene Mutation.

Eloisa Navarro1, Clara De Andrés1, Carmen Guerrero2, Santiago Giménez-Roldán1.   

Abstract

BACKGROUND: Alzheimer's disease (AD) is the second-most frequent cause underlying corticobasal syndrome (CBS). However, a reliable diagnosis using clinical, neuropsychological, or neuroimaging approaches has not yet been achieved.
METHODS: Clinical, neuropsychological, imaging, and neuropathology studies were undertaken in a large Spanish family with early-onset familial AD (EOFAD) carrying a Met233Leu mutation linked to presenilin-1 gene (PSEN-1).
RESULTS: Two of three examined members of this family presented with the usual amnestic pattern. At the age of 47 years, a third family member, in whom pathology was later confirmed, developed prominent CBS combined with severe neuropsychiatric and behavioral disturbances resembling those often found in EOFAD.
CONCLUSION: Although CBS in EOFAD appears to be rare, demonstration of a linkage to PSEN-1 gene mutations may permit in vivo diagnosis.

Entities:  

Keywords:  corticobasal syndrome; early‐onset familial Alzheimer's disease; genetics; presenilin‐1

Year:  2015        PMID: 30838239      PMCID: PMC6353493          DOI: 10.1002/mdc3.12212

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN: 2330-1619


  52 in total

Review 1.  Corticobasal degeneration look-alikes.

Authors:  K P Bhatia; M S Lee; J O Rinne; T Revesz; F Scaravilli; L Davies; C D Marsden
Journal:  Adv Neurol       Date:  2000

2.  A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset.

Authors:  A Tedde; P Forleo; B Nacmias; C Piccini; L Bracco; S Piacentini; S Sorbi
Journal:  Neurology       Date:  2000-11-28       Impact factor: 9.910

3.  Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation.

Authors:  G Raux; R Gantier; C Thomas-Anterion; J Boulliat; P Verpillat; D Hannequin; A Brice; T Frebourg; D Campion
Journal:  Neurology       Date:  2000-11-28       Impact factor: 9.910

4.  DGGE method for the mutational analysis of the coding and proximal promoter regions of the Alzheimer's disease presenilin-1 gene: two novel mutations.

Authors:  J Aldudo; M J Bullido; F Valdivieso
Journal:  Hum Mutat       Date:  1999       Impact factor: 4.878

5.  Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations.

Authors:  E A Rogaeva; K C Fafel; Y Q Song; H Medeiros; C Sato; Y Liang; E Richard; E I Rogaev; P Frommelt; A D Sadovnick; W Meschino; K Rockwood; M A Boss; R Mayeux; P St George-Hyslop
Journal:  Neurology       Date:  2001-08-28       Impact factor: 9.910

6.  A brief cognitive test battery to differentiate Alzheimer's disease and frontotemporal dementia.

Authors:  P S Mathuranath; P J Nestor; G E Berrios; W Rakowicz; J R Hodges
Journal:  Neurology       Date:  2000-12-12       Impact factor: 9.910

7.  The FAB: a Frontal Assessment Battery at bedside.

Authors:  B Dubois; A Slachevsky; I Litvan; B Pillon
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8.  Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations.

Authors:  H Houlden; M Baker; E McGowan; P Lewis; M Hutton; R Crook; N W Wood; S Kumar-Singh; J Geddes; M Swash; F Scaravilli; J L Holton; T Lashley; T Tomita; T Hashimoto; A Verkkoniemi; H Kalimo; M Somer; A Paetau; J J Martin; C Van Broeckhoven; T Golde; J Hardy; M Haltia; T Revesz
Journal:  Ann Neurol       Date:  2000-11       Impact factor: 10.422

9.  Pathologic heterogeneity in clinically diagnosed corticobasal degeneration.

Authors:  B F Boeve; D M Maraganore; J E Parisi; J E Ahlskog; N Graff-Radford; R J Caselli; D W Dickson; E Kokmen; R C Petersen
Journal:  Neurology       Date:  1999-09-11       Impact factor: 9.910

10.  A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures.

Authors:  M Ezquerra; C Carnero; R Blesa; J L Gelpí; F Ballesta; R Oliva
Journal:  Neurology       Date:  1999-02       Impact factor: 9.910

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  2 in total

Review 1.  Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review.

Authors:  Federica Arienti; Giulia Lazzeri; Maria Vizziello; Edoardo Monfrini; Nereo Bresolin; Maria Cristina Saetti; Marina Picillo; Giulia Franco; Alessio Di Fonzo
Journal:  Cells       Date:  2021-01-15       Impact factor: 6.600

Review 2.  Neuropathology and emerging biomarkers in corticobasal syndrome.

Authors:  Shunsuke Koga; Keith A Josephs; Ikuko Aiba; Mari Yoshida; Dennis W Dickson
Journal:  J Neurol Neurosurg Psychiatry       Date:  2022-06-13       Impact factor: 13.654

  2 in total

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