Literature DB >> 16969157

Recent advances in hereditary sensory and autonomic neuropathies.

Kristien Verhoeven1, Vincent Timmerman, Barbara Mauko, Thomas R Pieber, Peter De Jonghe, Michaela Auer-Grumbach.   

Abstract

PURPOSE OF REVIEW: This review summarizes the genetic advances of hereditary sensory neuropathies and hereditary sensory and autonomic neuropathies, and provides information on phenotype-genotype correlation and on possible underlying pathomechanisms. RECENT
FINDINGS: Hereditary sensory neuropathies, also known as hereditary sensory and autonomic neuropathies, are a clinically and genetically heterogeneous group of disorders. These disorders are characterized by prominent sensory loss with acro-mutilating complications and a variable degree of motor and autonomic disturbances. Based on age at onset, clinical features and mode of inheritance, these disorders have originally been subdivided into five types. The identification of eight loci and six disease-causing genes for this group of disorders, however, has shown that this present classification has to be refined.
SUMMARY: This review will discuss each of the different loci and genes of these disorders, showing glimpses into a possible underlying pathomechanism leading to the degeneration of sensory and autonomic neurons.

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Year:  2006        PMID: 16969157     DOI: 10.1097/01.wco.0000245370.82317.f6

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  18 in total

Review 1.  Hereditary Sensory and Autonomic Neuropathies: Adding More to the Classification.

Authors:  Coreen Schwartzlow; Mohamed Kazamel
Journal:  Curr Neurol Neurosci Rep       Date:  2019-06-20       Impact factor: 5.081

2.  Mitochondrial protein alterations in a familial peripheral neuropathy caused by the V144D amino acid mutation in the sphingolipid protein, SPTLC1.

Authors:  Scott E Stimpson; Jens R Coorssen; Simon J Myers
Journal:  J Chem Biol       Date:  2014-11-14

3.  Congenital insensitivity to pain with anhidrosis in Sudanese children.

Authors:  Suhair A Othman; Amel A Malik
Journal:  Sudan J Paediatr       Date:  2016

4.  Increased lipid droplet accumulation associated with a peripheral sensory neuropathy.

Authors:  Lee L Marshall; Scott E Stimpson; Ryan Hyland; Jens R Coorssen; Simon J Myers
Journal:  J Chem Biol       Date:  2014-03-23

5.  TNF-α/TNFR1 signaling is required for the development and function of primary nociceptors.

Authors:  Michael A Wheeler; Danielle L Heffner; Suemin Kim; Sarah M Espy; Anthony J Spano; Corey L Cleland; Christopher D Deppmann
Journal:  Neuron       Date:  2014-05-07       Impact factor: 17.173

6.  Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9.

Authors:  Voraluck Phatarakijnirund; Steven Mumm; William H McAlister; Deborah V Novack; Deborah Wenkert; Karen L Clements; Michael P Whyte
Journal:  Bone       Date:  2015-12-31       Impact factor: 4.398

7.  Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.

Authors:  Masoud Shekarabi; Nathalie Girard; Jean-Baptiste Rivière; Patrick Dion; Martin Houle; André Toulouse; Ronald G Lafrenière; Freya Vercauteren; Pascale Hince; Janet Laganiere; Daniel Rochefort; Laurence Faivre; Mark Samuels; Guy A Rouleau
Journal:  J Clin Invest       Date:  2008-07       Impact factor: 14.808

8.  A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated.

Authors:  Thorsten Hornemann; Anke Penno; Stephane Richard; Garth Nicholson; Fleur S van Dijk; Annelies Rotthier; Vincent Timmerman; Arnold von Eckardstein
Journal:  Neurogenetics       Date:  2009-01-09       Impact factor: 2.660

9.  Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.

Authors:  Beyhan Tüysüz; Fatih Bayrakli; Michael L DiLuna; Kaya Bilguvar; Yasar Bayri; Cengiz Yalcinkaya; Aysegul Bursali; Elif Ozdamar; Baris Korkmaz; Christopher E Mason; Ali K Ozturk; Richard P Lifton; Matthew W State; Murat Gunel
Journal:  Neurogenetics       Date:  2008-03-06       Impact factor: 2.660

10.  Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.

Authors:  Annelies Rotthier; Jonathan Baets; Els De Vriendt; An Jacobs; Michaela Auer-Grumbach; Nicolas Lévy; Nathalie Bonello-Palot; Sara Sebnem Kilic; Joachim Weis; Andrés Nascimento; Marielle Swinkels; Moyo C Kruyt; Albena Jordanova; Peter De Jonghe; Vincent Timmerman
Journal:  Brain       Date:  2009-08-03       Impact factor: 13.501

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