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1.
J Parkinsons Dis ; 14(4): 873-881, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38759024

RESUMO

Cannabis (in all the varied methods of delivery) continues to garner significant attention as a potential therapeutic intervention for neurodegenerative disorders, including Parkinson's disease (PD). The recent legalization of personal use of cannabis products in some parts of the world has increased this interest and with it, potential availability to many more people. However, such access has led to more questions than answers for both patients and health care professionals. These include what symptom(s) of PD will cannabis products treat; what dose; what type of cannabis product to use and what are the side effects?


Assuntos
Maconha Medicinal , Doença de Parkinson , Humanos , Doença de Parkinson/tratamento farmacológico , Maconha Medicinal/efeitos adversos , Maconha Medicinal/administração & dosagem , Maconha Medicinal/uso terapêutico , Cannabis
3.
J Neurol Sci ; 347(1-2): 356-8, 2014 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-25456461

RESUMO

In this article, we describe three patients with different spinocerebellar ataxia (SCA) subtypes presenting with unusual movement disorders predominantly characterized by choreoathetosis, which, together with their autosomal dominant pattern of inheritance, resembled the Huntington-like syndromes. From a large SCA cohort, we have observed chorea in 1/35 SCA2, 1/112 SCA3/MJD, and 1/30 SCA7 patients. Twenty-eight patients with SCA1, 11 patients with SCA6, and 3 patients with SCA10 were also evaluated, and none of them presented chorea. We provide a brief report of the three cases, with a video demonstrating chorea. Although a debate regarding the frequency of chorea in SCA patients is a fact, its occurrence, together with the autosomal dominant pattern of inheritance, clearly imposes SCA in the differentials of Huntington-like syndromes. There is some debate about what to include in a list of Huntington-like disorders, with several review articles about Huntington-like syndromes not including SCA in the differential diagnosis, except for SCA17. We believe that SCAs-at least SCA1, SCA2, SCA3/MJD, SCA7 and DRPLA-should be thought in the diagnostic workout of at least the atypical cases, such as those presented in this report.


Assuntos
Doença de Huntington/diagnóstico , Ataxias Espinocerebelares/classificação , Ataxias Espinocerebelares/diagnóstico , Adulto , Idoso , Diagnóstico Diferencial , Feminino , Humanos , Doença de Huntington/genética , Doença de Huntington/fisiopatologia , Masculino , Pessoa de Meia-Idade , Proteínas do Tecido Nervoso/genética , Ataxias Espinocerebelares/genética , Ataxias Espinocerebelares/fisiopatologia , Síndrome
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