Literature DB >> 18616154

[Case of Charcot-Marie-Tooth disease type 1A with increased cerebrospinal fluid proteins and nerve root hypertrophy].

Noriko Ishigami1, Masaki Kondo, Masanori Nakagawa.   

Abstract

We report herein a 54-year-old man who first noticed muscle weakness of the hands and legs and hypesthesia of the legs at 20-years-old. Symptoms gradually worsened. Charcot-Marie-Tooth disease type 1A (CMT 1A) was diagnosed on the basis of a nerve conduction study and PMP22 gene duplication. Increased levels of cerebrospinal fluid proteins were identified and cervical and lumbosacral nerve root hypertrophy was evident on magnetic resonance imaging (MRI). CMT 1A with increased CSF proteins and nerve root hypertrophy was carefully evaluated clinically and electrophysiologically to rule out other motor sensory neuropathies such as CIDP. Increased levels of CSF proteins in this case might have resulted from circulatory disturbance of CSF in hypertrophic nerve roots.

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Year:  2008        PMID: 18616154     DOI: 10.5692/clinicalneurol.48.419

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN: 0009-918X


  4 in total

1.  Hidden Charcot-Marie-Tooth 1A as Revealed by Peripheral Nerve Imaging.

Authors:  Kazumoto Shibuya; Toshiki Yoshida; Sonoko Misawa; Yukari Sekiguchi; Minako Beppu; Hiroshi Amino; Yo-Ichi Suzuki; Tomoki Suichi; Atsuko Tsuneyama; Keigo Nakamura; Satoshi Kuwabara
Journal:  Intern Med       Date:  2019-07-10       Impact factor: 1.271

2.  Acute to Subacute Atraumatic Entrapment Neuropathies in Patients With CMT1A: A Report of a Distinct Phenotypic Variant of CMT1A.

Authors:  Zhiyong Chen; Monica Saini; Shermyn X M Neo; Peng-Soon Ng; Jasmine S Koh; Kalpana Prasad; Kamal Verma; Sonia Davila; Weng Khong Lim; Ziqun Phua; Michelle M Li; Corrine Kang; Karine S S Tay; Josiah Y H Chai
Journal:  Front Neurol       Date:  2022-02-25       Impact factor: 4.003

Review 3.  Clinical implications of genetic advances in Charcot-Marie-Tooth disease.

Authors:  Alexander M Rossor; James M Polke; Henry Houlden; Mary M Reilly
Journal:  Nat Rev Neurol       Date:  2013-09-10       Impact factor: 42.937

4.  Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan.

Authors:  Takaki Taniguchi; Masahiro Ando; Yuji Okamoto; Akiko Yoshimura; Yujiro Higuchi; Akihiro Hashiguchi; Kensuke Shiga; Arisa Hayashida; Taku Hatano; Hiroyuki Ishiura; Jun Mitsui; Nobutaka Hattori; Toshiki Mizuno; Masanori Nakagawa; Shoji Tsuji; Hiroshi Takashima
Journal:  Clin Genet       Date:  2020-11-27       Impact factor: 4.438

  4 in total

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