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Rinsho Shinkeigaku ; 56(2): 77-81, 2016.
Artículo en Japonés | MEDLINE | ID: mdl-26797478

RESUMEN

A 56-year-old man, who presented with 6 years history of difficulty in walking, was diagnosed as having vascular parkinsonism on the basis of the clinical findings of parkinsonism, pyramidal sign and the brain MRI findings of multiple lacunar infarction. Although he did not have hypertension, he had hyperhomocysteinemia and homozygous methylenetetrahydrofolate reductase (MTHFR) gene variant (C677T) as risk factors for ischemic stroke. Recent studies have shown that hyperhomocysteinemia and MTHFR gene variant are associated with small-vessel disease, suggesting that these risk factors may underlie vascular parkinsonism, particularly in patients lacking hypertension and in those with a relatively younger age at onset of this disease.


Asunto(s)
Variación Genética , Hiperhomocisteinemia/complicaciones , Metilenotetrahidrofolato Reductasa (NADPH2)/genética , Trastornos Parkinsonianos/diagnóstico , Trastornos Parkinsonianos/genética , Edad de Inicio , Humanos , Hipertensión , Masculino , Persona de Mediana Edad , Trastornos Parkinsonianos/etiología , Factores de Riesgo , Accidente Vascular Cerebral Lacunar/diagnóstico , Accidente Vascular Cerebral Lacunar/etiología
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