Literature DB >> 19443103

A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis.

Yasushi Iwasaki1, Mayuki Kizawa, Norio Hori, Tetsuyuki Kitamoto, Gen Sobue.   

Abstract

We describe the clinical features of a patient with Gerstmann-Sträussler-Scheinker syndrome with a mutation in the prion protein gene at codon 105 (GSS105) who presented with ataxia. Neurologic examination showed memory disturbance, dysarthria, extrapyramidal signs (bradykinesia and resting tremor) and ataxic gait without spasticity. Although GSS105 has been referred to as "spastic paraparesis-type GSS", the patient did not show spastic paraparesis or pyramidal signs, even 11 years after the onset of symptoms. Thus, the spectrum of the GSS105 phenotype varies among patients and requires further clinicopathologic elucidation.

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Year:  2009        PMID: 19443103     DOI: 10.1016/j.clineuro.2009.03.008

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN: 0303-8467            Impact factor:   1.876


  5 in total

1.  A Chinese Creutzfeldt-Jakob disease patient with E196K mutation in PRNP.

Authors:  Qi Shi; Cao Chen; Xiao-Nan Song; Chen Gao; Chan Tian; Wei Zhou; Xu-Hua Song; Lai-Shun Yao; Jun Han; Xiao-Ping Dong
Journal:  Prion       Date:  2011-04-01       Impact factor: 3.931

2.  Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases.

Authors:  Maya Higuma; Nobuo Sanjo; Katsuya Satoh; Yusei Shiga; Kenji Sakai; Ichiro Nozaki; Tsuyoshi Hamaguchi; Yosikazu Nakamura; Tetsuyuki Kitamoto; Susumu Shirabe; Shigeo Murayama; Masahito Yamada; Jun Tateishi; Hidehiro Mizusawa
Journal:  PLoS One       Date:  2013-03-28       Impact factor: 3.240

3.  Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrum.

Authors:  Kagari Koshi Mano; Takashi Matsukawa; Jun Mitsui; Hiroyuki Ishiura; Shin-Ichi Tokushige; Yuji Takahashi; Naoko Saito Sato; Fumiko Kusunoki Nakamoto; Yaeko Ichikawa; Yu Nagashima; Yasuo Terao; Jun Shimizu; Masashi Hamada; Yoshikazu Uesaka; Genko Oyama; Go Ogawa; Jun Yoshimura; Koichiro Doi; Shinichi Morishita; Shoji Tsuji; Jun Goto
Journal:  Neurol Genet       Date:  2016-01-07

Review 4.  Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases.

Authors:  Eva Bagyinszky; Vo Van Giau; Young Chul Youn; Seong Soo A An; SangYun Kim
Journal:  Neuropsychiatr Dis Treat       Date:  2018-08-14       Impact factor: 2.570

5.  An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid.

Authors:  Keisuke Ishizawa; Takashi Mitsufuji; Kei Shioda; Atsushi Kobayashi; Takashi Komori; Yoshihiko Nakazato; Tetsuyuki Kitamoto; Nobuo Araki; Toshimasa Yamamoto; Atsushi Sasaki
Journal:  Brain Behav       Date:  2018-09-21       Impact factor: 2.708

  5 in total

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