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1.
Brain Nerve ; 74(12): 1350-1353, 2022 Dec.
Artículo en Japonés | MEDLINE | ID: mdl-36503131

RESUMEN

Although currently it is known that neuronal hyperexcitability is the mechanism underlying epilepsy, this condition was previously associated with spiritual factors. Epilepsy surgery is considered in patients in whom administration of anti-seizure drugs is infeasible. Functional mapping of the brain and intraoperative monitoring have improved safety of epilepsy surgery. A ketogenic diet is considered in patients in whom surgery is not adaptive. The American made-for-television movie ...First Do No Harm (1997) highlights the usefulness of the ketogenic diet for intractable epilepsy. Notably, ketogenic diet therapy was approved for public health insurance coverage in Japan in 2016.


Asunto(s)
Dieta Cetogénica , Epilepsia Refractaria , Epilepsia , Humanos , Epilepsia Refractaria/cirugía , Epilepsia/tratamiento farmacológico , Epilepsia/cirugía , Cuerpos Cetónicos , Encéfalo , Resultado del Tratamiento
2.
Rinsho Shinkeigaku ; 61(3): 200-203, 2021 Mar 25.
Artículo en Japonés | MEDLINE | ID: mdl-33627582

RESUMEN

A 49-year-old woman with intellectual disability and a food preference for fried chicken entered a nursing home. After nursing home diet, she developed episodic attacks of hyperammonemic encephalopathy. Her characteristic food preference and the negative results for brain and liver imaging studies suggested urea cycle disorder. A high plasma citrulline level on amino acid analysis and a genetic test for citrine gene confirmed a citrine deficiency (adult-onset type II citrullinemia). Although a low-carbohydrate diet was insufficient, a combination therapy of a low-carbohydrate diet and a medium-chain triglyceride (MCT) oil was effective. MCT oil may be a promising treatment option.


Asunto(s)
Citrulinemia/tratamiento farmacológico , Citrulinemia/etiología , Casas de Salud , Triglicéridos/administración & dosificación , Citrulinemia/diagnóstico , Citrulinemia/genética , Diagnóstico Diferencial , Femenino , Heterocigoto , Humanos , Persona de Mediana Edad , Proteínas de Transporte de Membrana Mitocondrial/genética , Mutación , Aceites , Resultado del Tratamiento , Triglicéridos/química
3.
J Stroke Cerebrovasc Dis ; 30(1): 105432, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-33171423

RESUMEN

Moyamoya disease is a rare cerebrovascular disorder with unknown etiology and psychiatric symptoms occasionally manifest initially. Capgras syndrome is a unique neuropsychiatric symptom that is a delusional misidentification of a familiar person replaced by an identical imposter. We report the case of a 51-year-old woman with frontal lobe ischemic stroke caused by moyamoya disease, presenting with Capgras syndrome. Dysfunction of frontal areas may be attributable to development of Capgras syndrome.


Asunto(s)
Síndrome de Capgras/etiología , Lóbulo Frontal/irrigación sanguínea , Accidente Cerebrovascular Isquémico/etiología , Enfermedad de Moyamoya/complicaciones , Antipsicóticos/uso terapéutico , Síndrome de Capgras/diagnóstico , Síndrome de Capgras/tratamiento farmacológico , Síndrome de Capgras/psicología , Revascularización Cerebral , Femenino , Humanos , Accidente Cerebrovascular Isquémico/diagnóstico por imagen , Persona de Mediana Edad , Enfermedad de Moyamoya/diagnóstico por imagen , Enfermedad de Moyamoya/cirugía , Resultado del Tratamiento
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