scholarly journals Comparison of Huntington's Disease in Europe and North America

2016 ◽  
Vol 4 (3) ◽  
pp. 358-367 ◽  
Author(s):  
Michael Orth ◽  
Juliana Bronzova ◽  
Christine Tritsch ◽  
E. Ray Dorsey ◽  
Joaquim J. Ferreira ◽  
...  
Keyword(s):  
North America ◽  
Huntington's Disease ◽  
Huntington’S Disease

Huntington's disease-like 2 (HDL2) in North America and Japan

2004 ◽  
Vol 56 (5) ◽  
pp. 670-674 ◽  
Author(s):  
Russell L. Margolis ◽  
Susan E. Holmes ◽  
Adam Rosenblatt ◽  
Lisa Gourley ◽  
Elizabeth O'Hearn ◽  
...  
Keyword(s):  
North America ◽  
Huntington's Disease ◽  
Huntington’S Disease

Facts and figures about Huntington’s disease

2020 ◽  
pp. 1-8 ◽  
Author(s):  
Oliver Quarrell
Keyword(s):  
North America ◽  
Huntington's Disease ◽  
Huntington’S Disease ◽  
Original Description ◽  
The World ◽  
History Of ◽  
Different Parts

This chapter gives a brief history of Huntington’s disease (HD) starting with the original description by George Huntington. The prevalence of HD is discussed together with data variations in different parts of the world. For example the incidence of HD in Europe and North America is approximately 1 person in 10,000. Apart from humans, no other animal naturally develops HD. The condition can start at almost any age but it is more frequent in midlife. The duration of the disease can be very variable but 20 years is often given as an approximate average.

I29 Comparison of huntington’s disease in europe and North America

2016 ◽  
Vol 87 (Suppl 1) ◽  
pp. A68.4-A69
Author(s):  
Michael Orth ◽  
Juliana Bronzova ◽  
Christine Tritsch ◽  
Ray Dorsey ◽  
Joaquim J Ferreira ◽  
...  
Keyword(s):  
North America ◽  
Huntington's Disease ◽  
Huntington’S Disease

scholarly journals The Prevalence of Huntington's Disease

2016 ◽  
Vol 46 (2) ◽  
pp. 144-153 ◽  
Author(s):  
Michael D. Rawlins ◽  
Nancy S. Wexler ◽  
Alice R. Wexler ◽  
Sarah J. Tabrizi ◽  
Ian Douglas ◽  
...  
Keyword(s):  
North America ◽  
Huntington's Disease ◽  
Huntington’S Disease ◽  
Lower Incidence ◽  
Western Europe ◽  
The Past ◽  
Case Ascertainment ◽  
Asian Populations ◽  
The United Kingdom ◽  
Geographical Regions

Background: Reviews of the epidemiology of Huntington's disease (HD) suggest that its worldwide prevalence varies widely. This review was undertaken to confirm these observations, to assess the extent to which differences in case-ascertainment and/or diagnosis might be responsible, and to investigate whether the prevalence pattern has changed over the past 50 years. Methods: Eighty two relevant studies were identified from Medline and Embase, previous reviews, scrutiny of references from included and excluded studies and enquiry among those interested in the field. Results: The lowest rates were among the Asians and the highest among the Caucasians. The differences are not fully explained by varying approaches to case-ascertainment or diagnosis. There was evidence of an increasing prevalence of between 15 and 20% per decade in studies from Australia, North America and Western Europe. Conclusions: The prevalence of HD varies more than tenfold between different geographical regions. This variation can in part be attributed to differences in case-ascertainment and/or diagnostic criteria, but there is consistent evidence of a lower incidence in Asian populations. There is also evidence that in Australia, North America and in Western Europe (including the United Kingdom), prevalence has increased over the past 50 plus years.

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