Characteristics, pathophysiology and clinical management of weight loss in Huntington’s disease

2013 ◽  
Vol 3 (3) ◽  
pp. 253-266 ◽  
Author(s):  
N Ahmad Aziz ◽  
Raymund AC Roos
PLoS ONE ◽  
2021 ◽  
Vol 16 (7) ◽  
pp. e0253817
Author(s):  
Wasiq Khan ◽  
Sundus Alusi ◽  
Hissam Tawfik ◽  
Abir Hussain

Weight-loss is an integral part of Huntington’s disease (HD) that can start before the onset of motor symptoms. Investigating the underlying pathological processes may help in the understanding of this devastating disease as well as contribute to its management. However, the complex behavior and associations of multiple biological factors is impractical to be interpreted by the conventional statistics or human experts. For the first time, we combine a clinical dataset, expert knowledge and machine intelligence to model the multi-dimensional associations between the potentially relevant factors and weight-loss activity in HD, specifically at the premanifest stage. The HD dataset is standardized and transformed into required knowledge base with the help of clinical HD experts, which is then processed by the class rule mining and self-organising maps to identify the significant associations. Statistical results and experts’ report indicate a strong association between severe weight-loss in HD at the premanifest stage and measures of certain cognitive, psychiatric functional ability factors. These results suggest that the mechanism underlying weight-loss in HD is, at least partly related to dysfunction of certain areas of the brain, a finding that may have not been apparent otherwise. These associations will aid the understanding of the pathophysiology of the disease and its progression and may in turn help in HD treatment trials.


2020 ◽  
Vol 20 (6) ◽  
pp. 479-481
Author(s):  
Daniel Sabino De Oliveira ◽  
Daniela Pereira Santos ◽  
Daniel Oliveira Araujo ◽  
Pedro José Tomaselli ◽  
WIlson Marques Júnior ◽  
...  

A 67-year-old Brazilian man of African ancestry and his 60-year-old sister both presented with choreiform movements, although in the man these were significantly overshadowed by additional parkinsonism. The man also had a history of four epileptic seizures. Neurological examination in each also found slow saccades and a dysexecutive syndrome. Genetic tests for Huntington’s disease were negative but were positive for Huntington’s disease-like 2. There are various genetic causes of chorea diseases, and their correct identification is important for appropriate clinical management and genetic counselling.


2014 ◽  
Vol 22 (4) ◽  
pp. 797-810 ◽  
Author(s):  
Brett D Dufour ◽  
Catherine A Smith ◽  
Randall L Clark ◽  
Timothy R Walker ◽  
Jodi L McBride

2020 ◽  
pp. 9-23
Author(s):  
Oliver Quarrell

This chapter focuses mainly on the movement disorder, speech, balance, weight loss, swallowing, and speech. Chorea or purposeless involuntary movement is most commonly associated with HD. A patient may have a mixture of movement problems such as dystonia (abnormal posture), and bradykinesia (slowness of movement). The pattern of movement disorder may vary between people but frequently the dystonia and bradykinesia become more prominent as the disease progresses. As this happens more professionals may become involved in the care. It is important for the carer(s) to also take care of themselves.


2011 ◽  
Vol 44 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Jorien M.M. van der Burg ◽  
Annika Winqvist ◽  
N. Ahmad Aziz ◽  
Marion L.C. Maat-Schieman ◽  
Raymund A.C. Roos ◽  
...  

Author(s):  
Adam Rosenblatt ◽  
Karen Anderson ◽  
Alex D. Goumeniouk ◽  
Paul Lespérance ◽  
Martha A. Nance ◽  
...  

2008 ◽  
Vol 23 (11) ◽  
pp. 1491-1504 ◽  
Author(s):  
Wendy Phillips ◽  
Kathleen M. Shannon ◽  
Roger A. Barker

1992 ◽  
Vol 49 (4) ◽  
pp. 349-349 ◽  
Author(s):  
H. P. H. Kremer ◽  
R. A. C. Roos

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