Literature DB >> 15297793

Prevalence of inherited ataxias in the province of Padua, Italy.

M Zortea1, M Armani, E Pastorello, G F Nunez, S Lombardi, S Tonello, M T Rigoni, L Zuliani, M L Mostacciuolo, C Gellera, S Di Donato, C P Trevisan.   

Abstract

Few population studies are available on epidemiological indexes of hereditary ataxias. An investigation on the prevalence rate of these movement disorders is in progress for the Veneto region, the main area of northeast Italy with a population of 4,490,586 inhabitants. The first results of this epidemiological survey concern the province of Padua, which numbers 845,203 residents (January 1, 2002). The prevalence rate of inherited ataxias has been estimated at 93.3 cases per million inhabitants. The most common types appeared to be the autosomal dominant forms, namely spinocerebellar ataxia type 1 and 2, with a prevalence of 24 per 1,000,000. In the same population, with a prevalence rate of 6 per 1,000,000, Friedreich's ataxia was defined as the prominent recessive autosomal form. There were very rare cases of ataxia telangiectasia, ataxia with vitamin E deficiency and cerebellar ataxia with congenital muscular dystrophy, a recently identified autosomal recessive disease. 2004 S. Karger AG, Basel

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Year:  2004        PMID: 15297793     DOI: 10.1159/000080092

Source DB:  PubMed          Journal:  Neuroepidemiology        ISSN: 0251-5350            Impact factor:   3.282


  8 in total

1.  Autosomal recessive adult onset ataxia.

Authors:  Nataša Dragašević-Mišković; Iva Stanković; Andona Milovanović; Vladimir S Kostić
Journal:  J Neurol       Date:  2021-09-09       Impact factor: 4.849

Review 2.  Discovery of Therapeutics Targeting Oxidative Stress in Autosomal Recessive Cerebellar Ataxia: A Systematic Review.

Authors:  Sze Yuen Lew; Michael Weng Lok Phang; Pit Shan Chong; Jaydeep Roy; Chi Him Poon; Wing Shan Yu; Lee Wei Lim; Kah Hui Wong
Journal:  Pharmaceuticals (Basel)       Date:  2022-06-19

Review 3.  Essential tremor: the most common form of cerebellar degeneration?

Authors:  Elan D Louis; Phyllis L Faust
Journal:  Cerebellum Ataxias       Date:  2020-08-14

4.  Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management.

Authors:  M Anheim; M Fleury; B Monga; V Laugel; D Chaigne; G Rodier; E Ginglinger; C Boulay; S Courtois; N Drouot; M Fritsch; J P Delaunoy; D Stoppa-Lyonnet; C Tranchant; M Koenig
Journal:  Neurogenetics       Date:  2009-05-14       Impact factor: 2.660

5.  Sporadic ataxias in Japan--a population-based epidemiological study.

Authors:  Shoji Tsuji; Osamu Onodera; Jun Goto; Masatoyo Nishizawa
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

Review 6.  Pathogenic mechanisms underlying spinocerebellar ataxia type 1.

Authors:  Leon Tejwani; Janghoo Lim
Journal:  Cell Mol Life Sci       Date:  2020-04-18       Impact factor: 9.261

7.  Friedreich Ataxia: Diagnostic Yield and Minimal Frequency in South Brazil.

Authors:  Helena Fussiger; Maria Luiza Saraiva-Pereira; Sandra Leistner-Segal; Laura Bannach Jardim
Journal:  Cerebellum       Date:  2019-02       Impact factor: 3.847

8.  High relative frequency of SCA1 in Poland reflecting a potential founder effect.

Authors:  Wioletta Krysa; Anna Sulek; Maria Rakowicz; Walentyna Szirkowiec; Jacek Zaremba
Journal:  Neurol Sci       Date:  2016-05-19       Impact factor: 3.307

  8 in total

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