Literature DB >> 10210919

Hereditary sensory neuropathy with deafness and dementia: a clinical and neuroimaging study.

K Hojo1, T Imamura, M Takanashi, K Ishii, M Sasaki, S Imura, R Ozono, Y Takatsuki, S Takauchi, E Mori.   

Abstract

We describe three sibling patients with autosomal dominantly inherited sensory neuropathy, sensorineural hearing loss and dementia. The features of cognitive-behavioral deficits in the patients, including executive dysfunction, apathy, indifference and inattention, were consistent with a frontal lobe dysfunction. Magnetic resonance imaging showed a diffuse brain atrophy. A fluorodeoxyglucose positron emission tomography in one patient and a single photon emission computed tomography in another demonstrated a glucose hypometabolism or a hypoperfusion in the medial frontal and thalamic regions. Primary frontal involvement or frontal dysfunction secondary to thalamic lesions may contribute to the nature of dementia in these patients. Copyright 1999 Lippincott Williams & Wilkins

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Year:  1999        PMID: 10210919     DOI: 10.1046/j.1468-1331.1999.630357.x

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  8 in total

1.  A novel de novo exon 21 DNMT1 mutation causes cerebellar ataxia, deafness, and narcolepsy in a Brazilian patient.

Authors:  José Luiz Pedroso; Orlando Graziani Povoas Barsottini; Ling Lin; Atle Melberg; Acary S B Oliveira; Emmanuel Mignot
Journal:  Sleep       Date:  2013-08-01       Impact factor: 5.849

2.  Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.

Authors:  Juliane Winkelmann; Ling Lin; Barbara Schormair; Birgitte R Kornum; Juliette Faraco; Giuseppe Plazzi; Atle Melberg; Ferdinando Cornelio; Alexander E Urban; Fabio Pizza; Francesca Poli; Fabian Grubert; Thomas Wieland; Elisabeth Graf; Joachim Hallmayer; Tim M Strom; Emmanuel Mignot
Journal:  Hum Mol Genet       Date:  2012-02-09       Impact factor: 6.150

Review 3.  Germline Abnormalities in DNA Methylation and Histone Modification and Associated Cancer Risk.

Authors:  Jenna A Fernandez; Mrinal M Patnaik
Journal:  Curr Hematol Malig Rep       Date:  2022-06-02       Impact factor: 4.213

4.  Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E.

Authors:  Zhifu Sun; Yanhong Wu; Tamas Ordog; Saurabh Baheti; Jinfu Nie; Xiaohui Duan; Kaori Hojo; Jean-Pierre Kocher; Peter J Dyck; Christopher J Klein
Journal:  Epigenetics       Date:  2014-07-07       Impact factor: 4.528

5.  DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss.

Authors:  Christopher J Klein; Tom Bird; Nilufer Ertekin-Taner; Sarah Lincoln; Robert Hjorth; Yanhong Wu; John Kwok; Georges Mer; Peter J Dyck; Garth A Nicholson
Journal:  Neurology       Date:  2013-01-30       Impact factor: 9.910

6.  Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss.

Authors:  Christopher J Klein; Maria-Victoria Botuyan; Yanhong Wu; Christopher J Ward; Garth A Nicholson; Simon Hammans; Kaori Hojo; Hiromitch Yamanishi; Adam R Karpf; Douglas C Wallace; Mariella Simon; Cecilie Lander; Lisa A Boardman; Julie M Cunningham; Glenn E Smith; William J Litchy; Benjamin Boes; Elizabeth J Atkinson; Sumit Middha; P James B Dyck; Joseph E Parisi; Georges Mer; David I Smith; Peter J Dyck
Journal:  Nat Genet       Date:  2011-05-01       Impact factor: 38.330

7.  DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated?

Authors:  Alessandra Maresca; Mirko Zaffagnini; Leonardo Caporali; Valerio Carelli; Claudia Zanna
Journal:  Front Genet       Date:  2015-03-12       Impact factor: 4.599

Review 8.  Epigenetic regulation in the inner ear and its potential roles in development, protection, and regeneration.

Authors:  Wanda S Layman; Jian Zuo
Journal:  Front Cell Neurosci       Date:  2015-01-07       Impact factor: 5.505

  8 in total

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