Literature DB >> 21572052

Focal central white matter lesions in Alexander disease.

Pauline Barreau1, Morgan J Prust, Jeremy Crane, Johanna Loewenstein, Nadja Kadom, Adeline Vanderver.   

Abstract

Alexander disease is a neurodegenerative disorder of the central white matter caused by dominant mutations in GFAP, the gene encoding glial fibrillary acidic protein. Magnetic resonance imaging pattern recognition studies have established characteristic radiologic phenotypes for this disorder. In some cases, however, genetically confirmed cases do not express these features, and several reports have identified "atypical" radiologic findings in Alexander disease patients. Here, the authors report 3 genetically confirmed Alexander disease cases with focal central white matter lesions that, upon longitudinal clinical and radiologic evaluation, appear to reflect an atypical Alexander disease magnetic resonance imaging phenotype and not another pathophysiologic process such as encephalitis, infarction, or neoplasm.

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Year:  2011        PMID: 21572052      PMCID: PMC4154515          DOI: 10.1177/0883073811405381

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  3 in total

1.  Unusual variants of Alexander's disease.

Authors:  Marjo S van der Knaap; Gajja S Salomons; Rong Li; Emilio Franzoni; Luiz González Gutiérrez-Solana; Leo M E Smit; Richard Robinson; Collin D Ferrie; Bruce Cree; Alyssa Reddy; Neil Thomas; Brenda Banwell; Frederik Barkhof; Cornelis Jakobs; Anne Johnson; Albee Messing; Michael Brenner
Journal:  Ann Neurol       Date:  2005-03       Impact factor: 10.422

2.  Alexander disease: diagnosis with MR imaging.

Authors:  M S van der Knaap; S Naidu; S N Breiter; S Blaser; H Stroink; S Springer; J C Begeer; R van Coster; P G Barth; N H Thomas; J Valk; J M Powers
Journal:  AJNR Am J Neuroradiol       Date:  2001-03       Impact factor: 3.825

3.  Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease.

Authors:  M Brenner; A B Johnson; O Boespflug-Tanguy; D Rodriguez; J E Goldman; A Messing
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

  3 in total
  4 in total

1.  All in Your Mind? New-Onset Dysphagia in a Previously Healthy Adolescent Child.

Authors:  Jake Sequeira; Douglas Willson; Mark Marinello
Journal:  J Pediatr Intensive Care       Date:  2019-12-05

2.  CSF and Blood Levels of GFAP in Alexander Disease

Authors:  Paige L Jany; Guillermo E Agosta; William S Benko; Jens C Eickhoff; Stephanie R Keller; Wolfgang Köehler; David Koeller; Soe Mar; Sakkubai Naidu; Jayne Marie Ness; Davide Pareyson; Deborah L Renaud; Ettore Salsano; Raphael Schiffmann; Julie Simon; Adeline Vanderver; Florian Eichler; Marjo S van der Knaap; Albee Messing
Journal:  eNeuro       Date:  2015-10-01

Review 3.  Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing.

Authors:  Katayoun Heshmatzad; Niloofar Naderi; Tannaz Masoumi; Hamidreza Pouraliakbar; Samira Kalayinia
Journal:  Eur J Med Res       Date:  2022-09-10       Impact factor: 4.981

4.  Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma.

Authors:  Keren Machol; Joseph Jankovic; Dhanya Vijayakumar; Lindsay C Burrage; Mahim Jain; Richard A Lewis; Gregory N Fuller; Mingchu Xu; Marta Penas-Prado; Maria K Gule-Monroe; Jill A Rosenfeld; Rui Chen; Christine M Eng; Yaping Yang; Brendan H Lee; Paolo M Moretti; Shweta U Dhar
Journal:  Neurol Genet       Date:  2018-07-20
  4 in total

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