Literature DB >> 24685771

Brain magnetic resonance imaging findings and auditory brainstem response in a child with spastic paraplegia 2 due to a PLP1 splice site mutation.

Kazuo Kubota1, Yoshiaki Saito2, Chihiro Ohba3, Hirotomo Saitsu3, Tetsuhiro Fukuyama4, Akihiko Ishiyama1, Takashi Saito1, Hirofumi Komaki1, Eiji Nakagawa1, Kenji Sugai1, Masayuki Sasaki1, Naomichi Matsumoto3.   

Abstract

A boy with spastic paraplegia type 2 (SPG2) due to a novel splice site mutation of PLP1 presented with progressive spasticity of lower limbs, which was first observed during late infancy, when he gained the ability to walk with support. His speech was slow and he had dysarthria. The patient showed mildly delayed intellectual development. Subtotal dysmyelination in the central nervous system was revealed, which was especially prominent in structures known to be myelinated during earlier period, whereas structures that are myelinated later were better myelinated. These findings on the brain magnetic resonance imaging were unusual for subjects with PLP1 mutations. Peaks I and II of the auditory brainstem response (ABR) were normally provoked, but peaks III-V were not clearly demarcated, similarly to the findings in Pelizaeus-Merzbacher disease. These findings of brain MRI and ABR may be characteristic for a subtype of SPG2 patients.
Copyright © 2014 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Auditory brainstem response; Dysmyelination; PLP1; Pelizaeus–Merzbacher disease; Spastic paraplegia 2

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Year:  2014        PMID: 24685771     DOI: 10.1016/j.braindev.2014.03.001

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  2 in total

1.  Clinical and genetic study of hereditary spastic paraplegia in Canada.

Authors:  Nicolas Chrestian; Nicolas Dupré; Ziv Gan-Or; Anna Szuto; Shiyi Chen; Anil Venkitachalam; Jean-Denis Brisson; Jodi Warman-Chardon; Sohnee Ahmed; Setareh Ashtiani; Heather MacDonald; Noreen Mohsin; Karim Mourabit-Amari; Pierre Provencher; Kym M Boycott; Dimitri J Stavropoulos; Patrick A Dion; Peter N Ray; Oksana Suchowersky; Guy A Rouleau; Grace Yoon
Journal:  Neurol Genet       Date:  2016-12-05

2.  Cortical Damage Associated With Cognitive and Motor Impairment in Hereditary Spastic Paraplegia: Evidence of a Novel SPAST Mutation.

Authors:  Jian-Zhong Lin; Hong-Hua Zheng; Qi-Lin Ma; Chen Wang; Li-Ping Fan; Han-Ming Wu; Dan-Ni Wang; Jia-Xing Zhang; Yi-Hong Zhan
Journal:  Front Neurol       Date:  2020-05-27       Impact factor: 4.003

  2 in total

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