Sporadic corticobasal syndrome with progranulin mutation presenting as progressive apraxic agraphia

Archives of Neurology

Volumn 68, Issue 3, 2011, Pages 376-380

  Passov, Victoria ^a   Gavrilova, Ralitza H ^a   Strand, Edythe ^a   Cerhan, Jane H ^a   Josephs, Keith A ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORODEOXYGLUCOSE;

ADULT; AGRAPHIA; APRAXIC AGRAPHIA; ARTICLE; BASE PAIRING; BRAIN DISEASE; CASE REPORT; DISEASE COURSE; FEMALE; FRONTAL LOBE; GENE; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; HUMAN; MUTATIONAL ANALYSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PARIETAL LOBE; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; PROGRANULIN GENE; SPORADIC CORTICOBASAL SYNDROME;

AGRAPHIA; BASAL GANGLIA DISEASES; BRAIN; FEMALE; FLUORODEOXYGLUCOSE F18; FUNCTIONAL LATERALITY; HANDWRITING; HUMANS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; MUTATION; NEUROPSYCHOLOGICAL TESTS; POSITRON-EMISSION TOMOGRAPHY; RADIOPHARMACEUTICALS;

EID: 79952595988     PISSN: 00039942     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneurol.2011.26     Document Type: Article

References (15)

1. Valenstein E, Heilman KM. Apraxic agraphia with neglect-induced paragraphia. Arch Neurol. 1979;36(8):506-508. (Pubitemid 9188003)
2. Heilman KM, Coenen A, Kluger B. Progressive asymmetric apraxic agraphia. Cogn Behav Neurol. 2008;21(1):14-17. (Pubitemid 351355037)
3. Kokmen E, Naessens JM, Offord KP. A short test of mental status: description and preliminary results. Mayo Clin Proc. 1987;62(4):281-288. (Pubitemid 17052827)
4. Lezak MD. Neuropsychological Assessment. New York, NY: Oxford University Press; 1995.
5. Whitwell JL, Jack CR Jr, Baker M, et al. Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations. Arch Neurol. 2007;64(3):371-376. (Pubitemid 46425691)
6. Whitwell JL, Jack CR Jr, Boeve BF, et al. Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN. Neurology. 2009;72(9):813-820.
7. Gass J, Cannon A, Mackenzie IR, et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet. 2006; 15(20):2988-3001. (Pubitemid 44530703)
8. Yu CE, Bird TD, Bekris LM, et al. The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration. Arch Neurol. 2010; 67(2):161-170.
9. Josephs KA, Ahmed Z, Katsuse O, et al. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations. J Neuropathol Exp Neurol. 2007;66(2):142-151. (Pubitemid 46208735)
10. Josephs KA, Petersen RC, Knopman DS, et al. Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP. Neurology. 2006;66(1):41-48. (Pubitemid 43739589)
11. Hu WT, Rippon GW, Boeve BF, et al. Alzheimer's disease and corticobasal degeneration presenting as corticobasal syndrome. Mov Disord. 2009;24(9):1375-1379.
12. Coslett HB, Gonzales Rothi LJ, Valenstein E, Heilman KM. Dissociations of writing and praxis: two cases in point. Brain Lang. 1986;28(2):357-369. (Pubitemid 16003300)
13. Basso A, Taborelli A, Vignolo LA. Dissociated disorders of speaking and writing in aphasia. J Neurol Neurosurg Psychiatry. 1978;41(6):556-563. (Pubitemid 8359585)
14. Boeve BF, Lang AE, Litvan I. Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia. Ann Neurol. 2003; 54(suppl 5):S15-S19. (Pubitemid 36760148)
15. Josephs KA, Duffy JR, Strand EA, et al. Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech. Brain. 2006;129(pt 6):1385-1398. (Pubitemid 43999372)