Literature DB >> 12529785

Clinical features and molecular genetics of hereditary peripheral neuropathies.

Gregor Kuhlenbäumer1, Peter Young, Gert Hünermund, Bernd Ringelstein, Florian Stögbauer.   

Abstract

Hereditary peripheral neuropathies are the most common monogenetically inherited diseases of the nervous system. The prevalence of the Hereditary Motor and Sensory Neuropathy Type 1A (HMSN 1A or Charcot-Marie-Tooth Neuropathy 1A, CMT1A) alone is estimated to be as high as 1/5000. In 1991, a duplication on chromosome 17p11.2 was identified as the causative genetic defect of CMT1A. Since then causative mutations in 17 genes have been identified. This review summarises the clinical and molecular genetic features of primary inherited neuropathies. It is aimed primarily at clinicians and geneticists. Therefore less emphasis is placed on the pathology and the (often unknown) underlying biological disease mechanisms.

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Year:  2002        PMID: 12529785     DOI: 10.1007/s00415-002-0946-3

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  10 in total

Review 1.  Myelin disorders: Causes and perspectives of Charcot-Marie-Tooth neuropathy.

Authors:  Gerd Meyer zu Hörste; Thomas Prukop; Klaus-Armin Nave; Michael W Sereda
Journal:  J Mol Neurosci       Date:  2006       Impact factor: 3.444

2.  Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease with phenotypic variability.

Authors:  G Karadima; M Panas; P Floroskufi; N Kalfakis; D Vassilopoulos
Journal:  J Neurol       Date:  2005-08-17       Impact factor: 4.849

3.  A new form of congenital proprioceptive sensory neuropathy associated with arthrogryposis multiplex.

Authors:  Hiroshi Shibasaki; Takefumi Hitomi; Takahiro Mezaki; Takeshi Kihara; Hidekazu Tomimoto; Akio Ikeda; Shun Shimohama; Masatoshi Ito; Nobuyuki Oka
Journal:  J Neurol       Date:  2004-11       Impact factor: 4.849

4.  Defective axonal transport of Rab7 GTPase results in dysregulated trophic signaling.

Authors:  Kai Zhang; Rotem Fishel Ben Kenan; Yasuko Osakada; Wei Xu; Rachel S Sinit; Liang Chen; Xiaobei Zhao; Jia-Yun Chen; Bianxiao Cui; Chengbiao Wu
Journal:  J Neurosci       Date:  2013-04-24       Impact factor: 6.167

5.  Positively charged residues within the MYO19 MyMOMA domain are essential for proper localization of MYO19 to the mitochondrial outer membrane.

Authors:  Jenci L Hawthorne; Prachi R Mehta; Pali P Singh; Nathan Q Wong; Omar A Quintero
Journal:  Cytoskeleton (Hoboken)       Date:  2016-05-24

6.  Pharmacological induction of the heat shock response improves myelination in a neuropathic model.

Authors:  Sunitha Rangaraju; Irina Madorsky; Jocelyn Go Pileggi; Adeela Kamal; Lucia Notterpek
Journal:  Neurobiol Dis       Date:  2008-07-08       Impact factor: 5.996

7.  Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2).

Authors:  Kathrin Engelfried; Matthias Vorgerd; Michaela Hagedorn; Gerhard Haas; Jürgen Gilles; Jörg T Epplen; Moritz Meins
Journal:  BMC Med Genet       Date:  2006-06-08       Impact factor: 2.103

Review 8.  Management of Charcot-Marie-Tooth disease: improving long-term care with a multidisciplinary approach.

Authors:  Donald McCorquodale; Evan M Pucillo; Nicholas E Johnson
Journal:  J Multidiscip Healthc       Date:  2016-01-19

9.  Fatigue, reduced sleep quality and restless legs syndrome in Charcot-Marie-Tooth disease: a web-based survey.

Authors:  Matthias Boentert; Rainer Dziewas; Anna Heidbreder; Svenja Happe; Ilka Kleffner; Stefan Evers; Peter Young
Journal:  J Neurol       Date:  2009-11-24       Impact factor: 4.849

Review 10.  Sleep and sleep disorders in rare hereditary diseases: a reminder for the pediatrician, pediatric and adult neurologist, general practitioner, and sleep specialist.

Authors:  Natan Gadoth; Arie Oksenberg
Journal:  Front Neurol       Date:  2014-07-17       Impact factor: 4.003

  10 in total

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