Literature DB >> 3759416

Prevalence of hereditary ataxias and paraplegias in the province of Torino, Italy.

F Brignolio, M Leone, A Tribolo, M G Rosso, P Meineri, D Schiffer.   

Abstract

A descriptive epidemiological survey of hereditary ataxias and spastic paraplegias was conducted in the province of Torino, Italy (2,327 996 inhabitants). On prevalence day (31 December 1982) 142 patients were alive. Total prevalence was 6.1 cases/100,000 inhabitants (95% confidence limits = 5.1-7.0). The prevalence rate was 2.6 for recessive or sporadic juvenile ataxias, 1.3 for spastic paraplegias, 1.2 for autosomal dominant cerebellar ataxias, and 1.1 for late onset cerebellar ataxias. The prevalence of hereditary ataxias is similar in our province to that recorded in other populations, but hereditary spastic paraplegias are less frequent than in other populations.

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Year:  1986        PMID: 3759416     DOI: 10.1007/bf02283021

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  15 in total

1.  Clinical description and roentgenologic evaluation of patients with Friedreich's ataxia.

Authors:  G Geoffroy; A Barbeau; G Breton; B Lemieux; M Aube; C Leger; J P Bouchard
Journal:  Can J Neurol Sci       Date:  1976-11       Impact factor: 2.104

2.  Friedreich's ataxia in Western Norway.

Authors:  H Skre
Journal:  Clin Genet       Date:  1975-04       Impact factor: 4.438

3.  Adult-onset hereditary ataxia in Scotland.

Authors:  A H Koeppen; M B Hans; D I Shepherd; P V Best
Journal:  Arch Neurol       Date:  1977-10

4.  [Scientific raisins from 125 years SMW (Swiss Medical Weekly). Contribution to constitutional and hereditary research with the help of studies on hereditary ataxia (46 new cases of Friedreich's disease). 1923].

Authors:  E Hanhart
Journal:  Schweiz Med Wochenschr       Date:  1995-06-10

5.  Hereditary spastic paraplegia in Western Norway.

Authors:  H Skre
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

6.  Prevalence and occurrence of some rare neurological diseases in Iceland.

Authors:  K R Gudmundsson
Journal:  Acta Neurol Scand       Date:  1969       Impact factor: 3.209

7.  Patterns of neurologic diseases on guam.

Authors:  K M Chen; J A Brody; L T Kurland
Journal:  Arch Neurol       Date:  1968-12

8.  Classification of the hereditary ataxias and paraplegias.

Authors:  A E Harding
Journal:  Lancet       Date:  1983-05-21       Impact factor: 79.321

9.  The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

Authors:  A E Harding
Journal:  Brain       Date:  1982-03       Impact factor: 13.501

10.  A tentative classification of recessively inherited ataxias.

Authors:  A Barbeau
Journal:  Can J Neurol Sci       Date:  1982-05       Impact factor: 2.104

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  6 in total

1.  The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland.

Authors:  P McMonagle; S Webb; M Hutchinson
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-01       Impact factor: 10.154

2.  Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy.

Authors:  A Filla; G De Michele; R Marconi; L Bucci; C Carillo; A E Castellano; L Iorio; C Kniahynicki; F Rossi; G Campanella
Journal:  J Neurol       Date:  1992-07       Impact factor: 4.849

Review 3.  Degenerative Ataxias: challenges in clinical research.

Authors:  Sub H Subramony
Journal:  Ann Clin Transl Neurol       Date:  2016-11-17       Impact factor: 4.511

4.  The high prevalence of hereditary spastic paraplegia in Sardinia, insular Italy.

Authors:  Loretta Racis; Alessandra Tessa; Roberto Di Fabio; Eugenia Storti; Virgilio Agnetti; Carlo Casali; Filippo M Santorelli; Maura Pugliatti
Journal:  J Neurol       Date:  2013-10-20       Impact factor: 4.849

5.  Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP).

Authors:  Kathrin N Karle; Rebecca Schüle; Stephan Klebe; Susanne Otto; Christian Frischholz; Inga Liepelt-Scarfone; Ludger Schöls
Journal:  Orphanet J Rare Dis       Date:  2013-10-09       Impact factor: 4.123

6.  An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15.

Authors:  Geert Vander Stichele; Alexandra Durr; Grace Yoon; Rebecca Schüle; Craig Blackstone; Giovanni Esposito; Connor Buffel; Inês Oliveira; Christian Freitag; Stephane van Rooijen; Stéphanie Hoffmann; Leen Thielemans; Belinda S Cowling
Journal:  BMC Neurol       Date:  2022-03-24       Impact factor: 2.474

  6 in total

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