Literature DB >> 11342690

A major locus for several phenotypes of myoclonus--dystonia on chromosome 7q.

M Vidailhet1, J Tassin, F Durif, A Nivelon-Chevallier, Y Agid, A Brice, A Dürr.   

Abstract

Myoclonus--dystonia is a genetically heterogeneous autosomal dominant disorder caused by a mutation in the D2 dopamine receptor on chromosome 11 and a locus on chromosome 7q21-q31. The authors tested linkage to the chromosome 7q candidate region in four families with either myoclonic dystonia (n = 3) or essential myoclonus (n = 1). Age at onset ranged from 0.5 to 38 years. Only four patients from two families had a positive response to alcohol. Lod scores were positive in all four families, suggesting that chromosome 7q21-q31 is a major locus for myoclonus-dystonia with several phenotypes.

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Year:  2001        PMID: 11342690     DOI: 10.1212/wnl.56.9.1213

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

1.  Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia.

Authors:  Birgitt Müller; Katja Hedrich; Norman Kock; Natasa Dragasevic; Marina Svetel; Jennifer Garrels; Olfert Landt; Matthias Nitschke; Peter P Pramstaller; Wolf Reik; Eberhard Schwinger; Jürgen Sperner; Laurie Ozelius; Vladimir Kostic; Christine Klein
Journal:  Am J Hum Genet       Date:  2002-11-20       Impact factor: 11.025

Review 2.  Genetic Aspects of Myoclonus-Dystonia Syndrome (MDS).

Authors:  Laila Rachad; Nadia El Kadmiri; Ilham Slassi; Hicham El Otmani; Sellama Nadifi
Journal:  Mol Neurobiol       Date:  2016-01-20       Impact factor: 5.590

3.  Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus-dystonia.

Authors:  Faiza Chbel; Hicham Charroute; Redouane Boulouiz; Hasna Hamdaoui; Houssein Mossafa; Houda Benrahma; Karim Ouldim
Journal:  Clin Case Rep       Date:  2022-03-17
  3 in total

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