Literature DB >> 21403024

Sporadic corticobasal syndrome with progranulin mutation presenting as progressive apraxic agraphia.

Victoria Passov1, Ralitza H Gavrilova, Edythe Strand, Jane H Cerhan, Keith A Josephs.   

Abstract

OBJECTIVE: To examine the relationship between progranulin gene mutation and apraxic agraphia.
DESIGN: Case report.
SETTING: Tertiary care medical center. PATIENT: A 49-year-old right-handed woman who presented with apraxic agraphia that progressed into the corticobasal syndrome.
RESULTS: This woman had no family history of neurodegenerative disease. Magnetic resonance imaging and fluorodeoxyglucose positron emission tomographic scans of her head revealed significant asymmetric frontoparietal abnormalities, in keeping with the clinical diagnosis of corticobasal syndrome. Progranulin gene sequencing identified a 4-base pair deletion.
CONCLUSIONS: Patients presenting with early apraxic agraphia, a progressive disease course, and asymmetric frontoparietal abnormalities on brain scans should be considered for progranulin gene testing despite negative family history.

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Year:  2011        PMID: 21403024     DOI: 10.1001/archneurol.2011.26

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  7 in total

1.  A Case of Apraxic Agraphia in a Patient With Progressive Supranuclear Palsy.

Authors:  Giorgia Sciacca; Tiziana Maci; Giovanni Mostile; Maria Luisa Capuana; Antonina Luca; Loredana Raciti; Cristina Sanfilippo; Francesco Le Pira; Alessandra Nicoletti; Mario Zappia
Journal:  Mov Disord Clin Pract       Date:  2015-03-30

2.  Progressive apraxic agraphia with micrographia presenting as corticobasal syndrome showing extensive Pittsburgh compound B uptake.

Authors:  Yasuhisa Sakurai; Kenji Ishii; Masahiro Sonoo; Yuko Saito; Shigeo Murayama; Atsushi Iwata; Kensuke Hamada; Izumi Sugimoto; Shoji Tsuji; Toru Mannen
Journal:  J Neurol       Date:  2013-04-16       Impact factor: 4.849

Review 3.  Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.

Authors:  Carmen Gasca-Salas; Mario Masellis; Edwin Khoo; Binit B Shah; David Fisman; Anthony E Lang; Galit Kleiner-Fisman
Journal:  PLoS One       Date:  2016-04-21       Impact factor: 3.240

Review 4.  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

5.  Language in corticobasal syndrome: a systematic review.

Authors:  Isabel Junqueira de Almeida; Marcela Lima Silagi; Jacy Bezerra Parmera; Sonia Maria Dozzi Brucki; Eliane Schochat
Journal:  Dement Neuropsychol       Date:  2021 Jan-Mar

6.  Motor features in posterior cortical atrophy and their imaging correlates.

Authors:  Natalie S Ryan; Timothy J Shakespeare; Manja Lehmann; Shiva Keihaninejad; Jennifer M Nicholas; Kelvin K Leung; Nick C Fox; Sebastian J Crutch
Journal:  Neurobiol Aging       Date:  2014-06-06       Impact factor: 4.673

7.  Novel GRN mutation presenting as an aphasic dementia and evolving into corticobasal syndrome.

Authors:  Hugo Botha; NiCole A Finch; Ralitza H Gavrilova; Mary M Machulda; Julie A Fields; Val J Lowe; Ronald C Petersen; Clifford R Jack; Christina M Dheel; Debra J Gearhart; David S Knopman; Rosa Rademakers; Bradley F Boeve
Journal:  Neurol Genet       Date:  2017-12-11
  7 in total

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