Literature DB >> 10483789

Evidence of widespread axonal pathology in Wolfram syndrome.

P Shannon1, L Becker, J Deck.   

Abstract

Wolfram syndrome, characterised by diabetes insipidus, diabetes mellitus, optic atrophy sensorineural deafness and acquired urinary tract abnormalities, is an hereditary neurodegenerative syndrome, the pathogenesis of which is unknown. We report the post-mortem findings on a patient with well-documented Wolfram syndrome. The brain showed severe degeneration of the optic nerves, chiasm and tracts as well as severe loss of neurons from the lateral geniculate nuclei, basis pontis, and the hypothalamic paraventricular and supraoptic nuclei. In addition, there was a widespread axonal dystrophy with axonal swellings in the pontocerebellar tracts, the optic radiations, the hippocampal fornices and the deep cerebral white matter. This widespread axonal pathology parallels the pattern of neurodegeneration and in many areas is more striking than neuronal loss.

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Year:  1999        PMID: 10483789     DOI: 10.1007/s004010051084

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  10 in total

1.  Human iPSC-derived neurons reveal early developmental alteration of neurite outgrowth in the late-occurring neurodegenerative Wolfram syndrome.

Authors:  Sandra Pourtoy-Brasselet; Axel Sciauvaud; Maria-Gabriela Boza-Moran; Michel Cailleret; Margot Jarrige; Hélène Polvèche; Jérôme Polentes; Eric Chevet; Cécile Martinat; Marc Peschanski; Laetitia Aubry
Journal:  Am J Hum Genet       Date:  2021-10-25       Impact factor: 11.025

2.  Longitudinal Assessment of Neuroradiologic Features in Wolfram Syndrome.

Authors:  A Samara; H M Lugar; T Hershey; J S Shimony
Journal:  AJNR Am J Neuroradiol       Date:  2020-10-29       Impact factor: 3.825

3.  Wolfram syndrome: a clinicopathologic correlation.

Authors:  Justin B Hilson; Saumil N Merchant; Joe C Adams; Jeffrey T Joseph
Journal:  Acta Neuropathol       Date:  2009-05-16       Impact factor: 17.088

4.  Central nervous system PET-CT imaging reveals regional impairments in pediatric patients with Wolfram syndrome.

Authors:  Agnieszka Zmyslowska; Bogdan Malkowski; Wojciech Fendler; Maciej Borowiec; Karolina Antosik; Piotr Gnys; Dobromila Baranska; Wojciech Mlynarski
Journal:  PLoS One       Date:  2014-12-26       Impact factor: 3.240

5.  Diabetes mellitus, diabetes insipidus, optic atrophy, and deafness: A case of Wolfram (DIDMOAD) syndrome.

Authors:  Nasrollah Maleki; Bahman Bashardoust; Anahita Zakeri; Azita Salehifar; Zahra Tavosi
Journal:  J Curr Ophthalmol       Date:  2016-01-02

6.  Knockdown of wfs1, a fly homolog of Wolfram syndrome 1, in the nervous system increases susceptibility to age- and stress-induced neuronal dysfunction and degeneration in Drosophila.

Authors:  Yasufumi Sakakibara; Michiko Sekiya; Naoki Fujisaki; Xiuming Quan; Koichi M Iijima
Journal:  PLoS Genet       Date:  2018-01-22       Impact factor: 5.917

7.  Evidence for altered neurodevelopment and neurodegeneration in Wolfram syndrome using longitudinal morphometry.

Authors:  Heather M Lugar; Jonathan M Koller; Jerrel Rutlin; Sarah A Eisenstein; Olga Neyman; Anagha Narayanan; Ling Chen; Joshua S Shimony; Tamara Hershey
Journal:  Sci Rep       Date:  2019-04-12       Impact factor: 4.379

8.  Early brain vulnerability in Wolfram syndrome.

Authors:  Tamara Hershey; Heather M Lugar; Joshua S Shimony; Jerrel Rutlin; Jonathan M Koller; Dana C Perantie; Alex R Paciorkowski; Sarah A Eisenstein; M Alan Permutt
Journal:  PLoS One       Date:  2012-07-11       Impact factor: 3.240

9.  Modulation of wolframin expression in human placenta during pregnancy: comparison among physiological and pathological states.

Authors:  Angela Lucariello; Angelica Perna; Carmine Sellitto; Alfonso Baldi; Alessandro Iannaccone; Luigi Cobellis; Antonio De Luca; Maria De Falco
Journal:  Biomed Res Int       Date:  2014-01-23       Impact factor: 3.411

Review 10.  Developmental hypomyelination in Wolfram syndrome: new insights from neuroimaging and gene expression analyses.

Authors:  Amjad Samara; Rachel Rahn; Olga Neyman; Ki Yun Park; Ahmad Samara; Bess Marshall; Joseph Dougherty; Tamara Hershey
Journal:  Orphanet J Rare Dis       Date:  2019-12-03       Impact factor: 4.123

  10 in total

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