Literature DB >> 8005597

Anticipation in hereditary dentatorubral-pallidoluysian atrophy.

A Sano1, N Yamauchi, Y Kakimoto, O Komure, J Kawai, F Hazama, K Kuzume, N Sano, I Kondo.   

Abstract

Anticipation refers to the progressively earlier onset and increase in disease severity in successive generations. We studied four families with hereditary dentatorubral-pallidoluysian atrophy (DRPLA), a neurodegenerative disease, and anticipation was present in the mode of inheritance. In subsequent generations DRPLA shows an earlier onset and more severe as well as additional symptoms. Older onset patients suffer from cerebellar ataxia with or without dementia, whereas younger onset patients present as progressive myoclonus epilepsy syndrome, which consists of mental retardation, dementia, and cerebellar ataxia as well as epilepsy and myoclonus. Anticipation with paternal transmission was significantly greater than with maternal transmission.

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Year:  1994        PMID: 8005597     DOI: 10.1007/BF00201575

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  15 in total

1.  Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

Authors:  A R La Spada; E M Wilson; D B Lubahn; A E Harding; K H Fischbeck
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2.  A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group.

Authors: 
Journal:  Cell       Date:  1993-03-26       Impact factor: 41.582

3.  Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy.

Authors:  H Naito; S Oyanagi
Journal:  Neurology       Date:  1982-08       Impact factor: 9.910

4.  Anticipation in myotonic dystrophy: fact or fiction?

Authors:  C J Höweler; H F Busch; J P Geraedts; M F Niermeijer; A Staal
Journal:  Brain       Date:  1989-06       Impact factor: 13.501

5.  Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Authors:  M Mahadevan; C Tsilfidis; L Sabourin; G Shutler; C Amemiya; G Jansen; C Neville; M Narang; J Barceló; K O'Hoy
Journal:  Science       Date:  1992-03-06       Impact factor: 47.728

6.  Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

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Journal:  Cell       Date:  1991-12-20       Impact factor: 41.582

7.  Further segregation analysis of the fragile X syndrome with special reference to transmitting males.

Authors:  S L Sherman; P A Jacobs; N E Morton; U Froster-Iskenius; P N Howard-Peebles; K B Nielsen; M W Partington; G R Sutherland; G Turner; M Watson
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred.

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Journal:  Ann Neurol       Date:  1988-06       Impact factor: 10.422

9.  Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.

Authors:  I Kondo; H Ohta; M Yazaki; J E Ikeda; J F Gusella; I Kanazawa
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

10.  Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting.

Authors:  R M Ridley; C D Frith; L A Farrer; P M Conneally
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

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  8 in total

Review 1.  Pathological accumulation of atrophin-1 in dentatorubralpallidoluysian atrophy.

Authors:  Yasuyo Suzuki; Ikuru Yazawa
Journal:  Int J Clin Exp Pathol       Date:  2011-04-25

2.  Clinical and magnetic resonance imaging features of elderly onset dentatorubral-pallidoluysian atrophy.

Authors:  Atsuhiko Sugiyama; Noriko Sato; Yasuhiro Nakata; Yukio Kimura; Mikako Enokizono; Tomoko Maekawa; Madoka Kondo; Yuji Takahashi; Satoshi Kuwabara; Hiroshi Matsuda
Journal:  J Neurol       Date:  2017-12-13       Impact factor: 4.849

Review 3.  Molecular pathology of dentatorubral-pallidoluysian atrophy.

Authors:  I Kanazawa
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-06-29       Impact factor: 6.237

Review 4.  Genetic and Epigenetic Interplay Define Disease Onset and Severity in Repeat Diseases.

Authors:  Lise Barbé; Steve Finkbeiner
Journal:  Front Aging Neurosci       Date:  2022-05-03       Impact factor: 5.702

5.  Benign adult familial myoclonus epilepsy (BAFME): an autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) gene.

Authors:  A Kuwano; F Takakubo; Y Morimoto; E Uyama; M Uchino; M Ando; T Yasuda; A Terao; T Hayama; R Kobayashi; I Kondo
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

6.  Precise chromosomal locations of the genes for dentatorubral-pallidoluysian atrophy (DRPLA), von Willebrand factor (F8vWF) and parathyroid hormone-like hormone (PTHLH) in human chromosome 12p by deletion mapping.

Authors:  A Kuwano; Y Morimoto; T Nagai; Y Fukushima; H Ohashi; T Hasegawa; I Kondo
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

7.  Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy.

Authors:  M Connarty; N R Dennis; C Patch; J N Macpherson; J F Harvey
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

Review 8.  The Contribution of Somatic Expansion of the CAG Repeat to Symptomatic Development in Huntington's Disease: A Historical Perspective.

Authors:  Darren G Monckton
Journal:  J Huntingtons Dis       Date:  2021
  8 in total

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