Multiparity after an initial diagnosis of Parkinson's disease: a report on a rare case

2008 ◽  
Vol 90 (5) ◽  
pp. 2005.e1-2005.e2 ◽  
Author(s):  
Raimundo Nonato Campos-Sousa ◽  
Kelson James Almeida ◽  
Alesse Ribeiro dos Santos ◽  
Pedro Vitor Lopes-Costa ◽  
Benedito Borges da Silva
2021 ◽  
Vol 50 (11) ◽  
pp. 793-800
Author(s):  
Sophie Waller ◽  
Laura Williams ◽  
Hugo Morales-Briceño ◽  
Victor SC Fung

2010 ◽  
Vol 11 (3) ◽  
pp. B13-B14
Author(s):  
Marcy Tarrants ◽  
Maureen Lage ◽  
Marcy Tarrants ◽  
Jane Castelli-Haley

2005 ◽  
Vol 32 (6) ◽  
pp. 689-695 ◽  
Author(s):  
Diederick Stoffers ◽  
Jan Booij ◽  
Lisette Bosscher ◽  
Ania Winogrodzka ◽  
Erik C. Wolters ◽  
...  

2011 ◽  
Vol 26 (4) ◽  
pp. 653-658 ◽  
Author(s):  
Alexandra Gaenslen ◽  
Irene Swid ◽  
Inga Liepelt-Scarfone ◽  
Jana Godau ◽  
Daniela Berg

2014 ◽  
Vol 6 (2) ◽  
pp. 149-155 ◽  
Author(s):  
Teruyuki Takahashi ◽  
Masato Tamura ◽  
Keiichi Osabe ◽  
Takashi Tamiya ◽  
Kenji Miki ◽  
...  

2021 ◽  
Author(s):  
Mickael AUBIGNAT ◽  
Melissa Tir ◽  
Pierre Krystkowiak ◽  
Daniela Andriuta

Abstract Background: Episodic headaches with spontaneous hypothermia constitute an uncommon association and is not well recognized in the International Classification of Headache Disorders (ICHD-3). Spontaneous periodic hypothermia, also called Shapiro’s syndrome, is a rare disease characterized by hypothermia attacks associated or not with hyperhidrosis without any triggering factor.Case presentation: We report a rare case of Shapiro’s syndrome revealed by episodes of headache with spontaneous hypothermia with effectiveness of clonidine therapy in a 76-year-old Parkinson’s disease woman.Conclusions: In the literature, apart from Shapiro’s syndrome, headaches with hypothermia seem to occur very rarely. These symptoms may be considered as a very rare non-motor fluctuation of Parkinson’s disease.


2009 ◽  
Vol 124 (6) ◽  
pp. 668-673 ◽  
Author(s):  
E C Gan ◽  
D P Lau ◽  
K L Cheah

AbstractObjectives:(1) To present a rare case of stridor secondary to prolonged laryngospasm in a patient with Parkinson's disease, and (2) to review the literature on stridor in Parkinson's disease.Methods:We report a 73-year-old Parkinson's disease patient who developed acute stridor due to prolonged laryngospasm triggered by overspill of excessive secretions. The literature was reviewed, following a Medline search using the keywords ‘Parkinson's disease’ and ‘stridor’ or ‘airway obstruction’ or ‘laryngospasm’ or ‘laryngeal dystonia’ or ‘bilateral vocal cord palsy’.Result:Only 12 previously reported cases of stridor in Parkinson's disease patients were identified. Causes included bilateral vocal fold palsy (eight cases), laryngospasm (five), and dystonia of the jaw and neck muscles (two). The mechanism of laryngospasm in our patient was similar to ‘dry drowning’, and has not previously been described.Conclusion:Laryngospasm can be triggered in Parkinson's disease by excessive secretions entering the larynx. The mechanism is similar to ‘dry drowning’. Treatment focuses on reducing secretions. The use of botulinum toxin to reduce spasm is inappropriate in this situation. This case emphasises the importance of recognising different causes of stridor in Parkinson's disease patients, as this affects management.


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