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1.
Neurologia (Engl Ed) ; 38(2): 82-86, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-36402400

RESUMO

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant small-vessel disease caused by mutations of the NOTCH3 gene. It typically presents with migraine, recurrent brain ischaemia, and cognitive disorders. Seizures rarely present as the initial manifestation, with non-convulsive status epilepticus being even less frequent. We present a series of 3 related patients with this arteriopathy, 2 of whom presented status epilepticus as a manifestation of the disease.


Assuntos
CADASIL , Leucoencefalopatias , Estado Epiléptico , Humanos , CADASIL/complicações , CADASIL/diagnóstico , CADASIL/genética , Infarto Cerebral , Imageamento por Ressonância Magnética , Receptor Notch3/genética , Estado Epiléptico/etiologia
2.
Neurologia (Engl Ed) ; 2020 Oct 02.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33020014

RESUMO

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant small-vessel disease caused by mutations of the NOTCH3 gene. It typically presents with migraine, recurrent brain ischaemia, and cognitive disorders. Seizures rarely present as the initial manifestation, with non-convulsive status epilepticus being even less frequent. We present a series of 3 related patients with this arteriopathy, 2 of whom presented status epilepticus as a manifestation of the disease.

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