Literature DB >> 11359466

Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis.

G Siciliano1, M Manca, M Gennarelli, C Angelini, A Rocchi, A Iudice, M Miorin, M Mostacciuolo.   

Abstract

Before the discovery of the myotonic dystrophy (DM) gene, the DM epidemiological rates could not be accurately estimated. The aim of this study was to calculate the DM prevalence rates in Padova (North-East Italy) and in four provinces of North-West Tuscany (Central Italy) and, as of 30 June 1999, to do so using molecular genetic testing. A minimum prevalence rate of 9.31x10(-5) inhabitants was found, consistent with epidemiological rates worldwide, and more than two times as high as those of two previous studies conducted in the same areas during the era prior to molecular genetic testing. This study, the first in Italy since the discovery of the DM gene, underlines the importance of direct genetic diagnosis of DM, especially in detecting mildly affected patients, a fundamental step in correctly estimating the risk of disease transmission in affected families.

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Year:  2001        PMID: 11359466     DOI: 10.1034/j.1399-0004.2001.590508.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  13 in total

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Authors:  Hyun Sook Kim; Ki Wha Chung; Sung Hee Kang; Sung Kyung Choi; Sun Young Cho; Heasoo Koo; Sang-Beom Kim; Byung-Ok Choi
Journal:  Neurogenetics       Date:  2010-05-05       Impact factor: 2.660

Review 2.  Myotonic dystrophy.

Authors:  Charles A Thornton
Journal:  Neurol Clin       Date:  2014-06-06       Impact factor: 3.806

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Journal:  Neurol Sci       Date:  2010-09-15       Impact factor: 3.307

4.  Genetics correlates with lung function and nocturnal ventilation in myotonic dystrophy.

Authors:  Regina Monteiro; João Bento; Miguel R Gonçalves; Tiago Pinto; João Carlos Winck
Journal:  Sleep Breath       Date:  2013-01-15       Impact factor: 2.816

5.  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

6.  Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2.

Authors:  Vincenzo Romeo; E Pegoraro; C Ferrati; F Squarzanti; G Sorarù; A Palmieri; P Zucchetta; L Antunovic; E Bonifazi; G Novelli; C P Trevisan; M Ermani; R Manara; C Angelini
Journal:  J Neurol       Date:  2010-03-11       Impact factor: 4.849

7.  The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1.

Authors:  Alfonsina Ballester-Lopez; Ian Linares-Pardo; Emma Koehorst; Judit Núñez-Manchón; Guillem Pintos-Morell; Jaume Coll-Cantí; Miriam Almendrote; Giuseppe Lucente; Andrea Arbex; Jonathan J Magaña; Nadia M Murillo-Melo; Alejandro Lucia; Darren G Monckton; Sarah A Cumming; Alba Ramos-Fransi; Alicia Martínez-Piñeiro; Gisela Nogales-Gadea
Journal:  Genes (Basel)       Date:  2020-07-07       Impact factor: 4.096

8.  Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program.

Authors:  Nicholas E Johnson; Russell J Butterfield; Katie Mayne; Tara Newcomb; Carina Imburgia; Diane Dunn; Brett Duval; Marcia L Feldkamp; Robert B Weiss
Journal:  Neurology       Date:  2021-01-20       Impact factor: 9.910

9.  Epidemiology of muscular dystrophies in the Mediterranean area.

Authors:  Haluk Topaloglu
Journal:  Acta Myol       Date:  2013-12

Review 10.  Core Clinical Phenotypes in Myotonic Dystrophies.

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

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