Literature DB >> 9855541

Hereditary spastic paraplegia with a thin corpus callosum and thalamic involvement in Japan.

M Ueda1, Y Katayama, T Kamiya, M Mishina, H Igarashi, S Okubo, M Senda, K Iwabuchi, A Terashi.   

Abstract

The authors examined two Japanese siblings with a recessive hereditary spastic paraplegia (HSP) with dementia and a thin corpus callosum. Both showed thalamic glucose hypometabolism on PET. Recessive HSP with a thin corpus callosum is a rare disorder, with less than 20 reported patients, that may be a Japanese subtype of HSP.

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Year:  1998        PMID： 9855541     DOI： 10.1212/wnl.51.6.1751

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


  6 in total

1.  A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.

Authors:  Amir Boukhris; Imed Feki; Nizar Elleuch; Mohamed Imed Miladi; Anne Boland-Augé; Jérémy Truchetto; Emeline Mundwiller; Nadia Jezequel; Diana Zelenika; Chokri Mhiri; Alexis Brice; Giovanni Stevanin
Journal:  Neurogenetics       Date:  2010-07-01       Impact factor: 2.660

2.  Hereditary spastic paraplegia with a thin corpus callosum.

Authors:  Sivaraman Somasundaram; Seetharam Raghavendra; Atampreet Singh; Chandrasekharan Kesavadas; Muraleedharan Nair
Journal:  Pediatr Radiol       Date:  2007-03-27

3.  Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4.

Authors:  Francisco Grandas; Manuel Desco; Francisco J Navas-Sánchez; Alberto Fernández-Pena; Daniel Martín de Blas; Yasser Alemán-Gómez; Luís Marcos-Vidal; Juan A Guzmán-de-Villoria; Pilar Fernández-García; Julia Romero; Irene Catalina; Laura Lillo; José L Muñoz-Blanco; Andrés Ordoñez-Ugalde; Beatriz Quintáns; Julio Pardo; María-Jesús Sobrido; Susanna Carmona
Journal:  J Neurol       Date:  2021-01-28       Impact factor: 4.849

4.  Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutation.

Authors:  M-K Pan; S-C Huang; Y-C Lo; Chih-Chao Yang; T-W Cheng; Chi-Cheng Yang; M-S Hua; M-J Lee; W-Y I Tseng
Journal:  AJNR Am J Neuroradiol       Date:  2012-12-06       Impact factor: 3.825

5.  Mild cognitive impairment in novel SPG11 mutation-related sporadic hereditary spastic paraplegia with thin corpus callosum: case series.

Authors:  Chuan Li; Qi Yan; Feng-Ju Duan; Chao Zhao; Zhuo Zhang; Ying Du; Wei Zhang
Journal:  BMC Neurol       Date:  2021-01-11       Impact factor: 2.474

6.  An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions.

Authors:  Mika Hayakawa; Tomoyasu Matsubara; Yoko Mochizuki; Chisen Takeuchi; Motoyuki Minamitani; Masayuki Imai; Kenjiro Kosaki; Tomio Arai; Shigeo Murayama
Journal:  BMC Neurol       Date:  2022-01-03       Impact factor: 2.474
  6 in total

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