Literature DB >> 2924205

Origin and diffusion of the myotonic dystrophy gene in the Saguenay region (Quebec).

G Bouchard1, R Roy, M Declos, J Mathieu, K Kouladjian.   

Abstract

A very high prevalence (approximately 1/475 in 1985) of myotonic dystrophy (Steinert disease) is observed in the Saguenay region, which is located in the north-east part of the Province of Quebec. For various reasons, however, the literature on the subject generally associates a high degree of selective disadvantage with this gene, which seems to contradict the Saguenay data. Using a computerized regional population register, we have reconstituted patients' genealogies and family biographies. We have thus been able to study the origin of the gene and to compare the demographic behavior of patients and controls. On the whole, patients seem to be very little disadvantaged compared to controls, in terms of reproduction as well as of geographical and occupational mobility.

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Year:  1989        PMID: 2924205     DOI: 10.1017/s0317167100028651

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN: 0317-1671            Impact factor:   2.104


  6 in total

1.  Assessment of muscular strength and functional capacity in the juvenile and adult myotonic dystrophy type 1 population: a 3-year follow-up study.

Authors:  Marie-Pier Roussel; Marie-Michèle Fiset; Laurie Gauthier; Claudia Lavoie; Émilie McNicoll; Laurie Pouliot; Cynthia Gagnon; Elise Duchesne
Journal:  J Neurol       Date:  2021-04-27       Impact factor: 4.849

2.  Normal variation at the myotonic dystrophy locus in global human populations.

Authors:  C Zerylnick; A Torroni; S L Sherman; S T Warren
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

3.  Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.

Authors:  Tiina Suominen; Linda L Bachinski; Satu Auvinen; Peter Hackman; Keith A Baggerly; Corrado Angelini; Leena Peltonen; Ralf Krahe; Bjarne Udd
Journal:  Eur J Hum Genet       Date:  2011-03-02       Impact factor: 4.246

Review 4.  The Added Value of Cardiac Magnetic Resonance in Muscular Dystrophies.

Authors:  Mariana M Lamacie; Jodi Warman-Chardon; Andrew M Crean; Anca Florian; Karim Wahbi
Journal:  J Neuromuscul Dis       Date:  2019

5.  A More Efficient Transportable and Scalable System for Real-Time Activities and Exercises Recognition.

Authors:  Kévin Chapron; Valère Plantevin; Florentin Thullier; Kévin Bouchard; Elise Duchesne; Sébastien Gaboury
Journal:  Sensors (Basel)       Date:  2018-01-18       Impact factor: 3.576

Review 6.  Core Clinical Phenotypes in Myotonic Dystrophies.

Authors:  Stephan Wenninger; Federica Montagnese; Benedikt Schoser
Journal:  Front Neurol       Date:  2018-05-02       Impact factor: 4.003

  6 in total

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