Literature DB >> 15201379

Leucoencephalopathy with neuroaxonal spheroids (LENAS) presenting as the cerebellar subtype of multiple system atrophy.

M L Moro-de-Casillas1, M L Cohen, D E Riley.   

Abstract

Leucoencephalopathy with neuroaxonal spheroids (LENAS) is a rare disease of cerebral and cerebellar white matter. LENAS usually presents as a disorder of cognition and behaviour, or with gait dysfunction and ataxia. This report describes a patient who had a 14 year course of progressive neurological decline consistent with a clinical diagnosis of probable multiple system atrophy, with prominent cerebellar dysfunction and dysautonomia. Formal autonomic laboratory testing was consistent with global autonomic dysfunction of central origin. However, magnetic resonance imaging showed extensive white matter signal abnormalities, in addition to moderate cerebral and cerebellar atrophy. On postmortem microscopic examination, there were numerous axonal spheroids throughout the white matter of both regions. This case of LENAS presented unique clinical characteristics, and typical pathological findings.

Entities:  

Mesh:

Year:  2004        PMID: 15201379      PMCID: PMC1739090          DOI: 10.1136/jnnp.2003.028431

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  12 in total

1.  Sporadic diffuse leucoencephalopathy with axonal spheroids: report of a profuse and rapid cortical-spinal degeneration.

Authors:  A Maues De Paula; B Michel; D W Dickson; Z K Wszolek; J F Pellissier
Journal:  Neurol Sci       Date:  2011-10-18       Impact factor: 3.307

2.  Two cases of LENAS: diagnosis by MRI and biopsy.

Authors:  B Mayer; C Oelschlaeger; K Keyvani; T Niederstadt
Journal:  J Neurol       Date:  2007-08-21       Impact factor: 4.849

3.  Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids.

Authors:  J A Van Gerpen; C Wider; D F Broderick; D W Dickson; L A Brown; Z K Wszolek
Journal:  Neurology       Date:  2008-09-16       Impact factor: 9.910

Review 4.  Adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia: report of five cases and a new mutation.

Authors:  Kirk Kleinfeld; Bret Mobley; Peter Hedera; Adam Wegner; Subramaniam Sriram; Siddharama Pawate
Journal:  J Neurol       Date:  2012-09-30       Impact factor: 4.849

5.  Imaging features in conventional MRI, spectroscopy and diffusion weighted images of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS).

Authors:  Benjamin Bender; Uwe Klose; Tobias Lindig; Saskia Biskup; Thomas Nägele; Ludger Schöls; Kathrin N Karle
Journal:  J Neurol       Date:  2014-09-20       Impact factor: 4.849

6.  MRI characteristics and scoring in HDLS due to CSF1R gene mutations.

Authors:  Christina Sundal; Jay A Van Gerpen; Alexandra M Nicholson; Christian Wider; Elizabeth A Shuster; Jan Aasly; Salvatore Spina; Bernardino Ghetti; Sigrun Roeber; James Garbern; Anne Borjesson-Hanson; Alex Tselis; Russell H Swerdlow; Bradley B Miller; Shinsuke Fujioka; Michael G Heckman; Ryan J Uitti; Keith A Josephs; Matt Baker; Oluf Andersen; Rosa Rademakers; Dennis W Dickson; Daniel Broderick; Zbigniew K Wszolek
Journal:  Neurology       Date:  2012-07-25       Impact factor: 9.910

Review 7.  Rapid onset frontal leukodystrophy with decreased diffusion coefficient and neuroaxonal spheroids.

Authors:  Elisabeth Maillart; Audrey Rousseau; Damien Galanaud; Françoise Gray; Marc Polivka; Pierre Labauge; Jean-Jacques Hauw; Olivier Lyon-Caen; Olivier Gout; Frédéric Sedel
Journal:  J Neurol       Date:  2009-05-21       Impact factor: 4.849

Review 8.  Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD): a single entity?

Authors:  C Wider; J A Van Gerpen; S DeArmond; E A Shuster; D W Dickson; Z K Wszolek
Journal:  Neurology       Date:  2009-06-02       Impact factor: 9.910

9.  A novel mutation in CSF1R associated with hereditary diffuse leukoencephalopathy with spheroids.

Authors:  Qin Du; Minjin Wang; Hongyu Zhou
Journal:  Neurol Sci       Date:  2021-05-04       Impact factor: 3.307

10.  Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.

Authors:  Rosa Rademakers; Matt Baker; Alexandra M Nicholson; Nicola J Rutherford; NiCole Finch; Alexandra Soto-Ortolaza; Jennifer Lash; Christian Wider; Aleksandra Wojtas; Mariely DeJesus-Hernandez; Jennifer Adamson; Naomi Kouri; Christina Sundal; Elizabeth A Shuster; Jan Aasly; James MacKenzie; Sigrun Roeber; Hans A Kretzschmar; Bradley F Boeve; David S Knopman; Ronald C Petersen; Nigel J Cairns; Bernardino Ghetti; Salvatore Spina; James Garbern; Alexandros C Tselis; Ryan Uitti; Pritam Das; Jay A Van Gerpen; James F Meschia; Shawn Levy; Daniel F Broderick; Neill Graff-Radford; Owen A Ross; Bradley B Miller; Russell H Swerdlow; Dennis W Dickson; Zbigniew K Wszolek
Journal:  Nat Genet       Date:  2011-12-25       Impact factor: 38.330

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