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1.
J Neurosurg Anesthesiol ; 31(3): 285-290, 2019 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-29734272

RESUMO

The fragile X premutation is characterized by a repeat expansion mutation (between 55 to 200 CGG repeats) in the fragile X mental retardation 1 (FMR1) gene, which leads to RNA toxicity at the cellular level. This may cause patients with the premutation to be particularly susceptible to environmental toxins, which could manifest clinically as new or worsening ataxia and memory loss. Multiple published case reports have also suggested general anesthetics as a potential toxin leading to negative side effects when used in patients with fragile X-associated disorders. However, at this time, there have been no formal research studies regarding cellular changes or long-term clinical manifestations after general anesthetic use in this population. This review aims to highlight previous case reports regarding sequelae related to general anesthetic use in fragile X-associated disorders. New case reports related to this phenomenon are also included.


Assuntos
Anestesia Geral/métodos , Anestésicos Gerais , Síndrome do Cromossomo X Frágil/cirurgia , Anestesia Geral/efeitos adversos , Anestésicos Gerais/efeitos adversos , Humanos
2.
Neurol Neurochir Pol ; 50(4): 303-8, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27375149

RESUMO

We present the case of a 66-year-old man who has been treated for essential tremor since the age of 58. He developed mild cerebellar gait ataxia seven years after tremor onset. Moderate, global brain atrophy was identified on MRI scans. At the age of 68, only temporary tremor relief could be achieved by bilateral deep brain stimulation of the ventral intermedius nucleus of the thalamus. Bilateral stimulation of the subthalamic nucleus also resulted only in transient improvement. In the meantime, progressive gait ataxia and tetraataxia developed accompanied by other cerebellar symptoms, such as nystagmus and scanning speech. These correlated with progressive development of bilateral symmetric hyperintensity of the middle cerebellar peduncles on T2 weighted MRI scans. Genetic testing revealed premutation of the FMR1 gene, establishing the diagnosis of fragile X-associated tremor/ataxia syndrome. Although this is a rare disorder, it should be taken into consideration during preoperative evaluation of essential tremor. Postural tremor ceased two years later after thalamotomy on the left side, while kinetic tremor of the right hand also improved.


Assuntos
Ataxia/terapia , Estimulação Encefálica Profunda/métodos , Síndrome do Cromossomo X Frágil/terapia , Procedimentos Neurocirúrgicos/métodos , Tálamo/cirurgia , Tremor/terapia , Idoso , Ataxia/diagnóstico por imagem , Ataxia/fisiopatologia , Ataxia/cirurgia , Síndrome do Cromossomo X Frágil/diagnóstico por imagem , Síndrome do Cromossomo X Frágil/fisiopatologia , Síndrome do Cromossomo X Frágil/cirurgia , Humanos , Imageamento por Ressonância Magnética , Masculino , Núcleo Subtalâmico/diagnóstico por imagem , Núcleo Subtalâmico/fisiopatologia , Tálamo/diagnóstico por imagem , Tálamo/fisiopatologia , Resultado do Tratamento , Tremor/diagnóstico por imagem , Tremor/fisiopatologia , Tremor/cirurgia
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