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PMID: 2330114 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada).

Neurology ·Vol. 40 ·No. 5 ·1990-05-00 ·Pages 839-42

Mathieu J, De Braekeleer M, Prévost C

Abstract

The prevalence of myotonic dystrophy (MyD) in the Saguenay-Lac-Saint-Jean (SLSJ) region (Quebec, Canada) is 30 to 60 times the world's prevalence. We identified 746 patients (673 still alive) distributed in 88 families. Using a population-based register of the SLSJ area and several marriage repositories from northeastern Quebec, we could trace back all patients to a couple who settled in "Nouvelle-France" in 1657. The MyD gene was then passed on over 10 to 14 generations. This genealogical reconstruction is a strong argument in favor of the genetic homogeneity of MyD in the SLSJ region.

MeSH Terms
Female Humans Male Myotonic Dystrophy/epidemiology,genetics Pedigree Prevalence Quebec/epidemiology Surveys and Questionnaires
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Mathieu J
Clinique des maladies neuro-musculaires, Hôpital de Chicoutimi, PQ, Canada.
De Braekeleer M
Prévost C
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
Published
1990-05-00
Pages
839-42
Language
English
Region
United States
NLM ID
0401060
Subset
IM
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