Few studies focused on the long‐term outcome of Dravet syndrome in adulthood are
available in the literature, but all are concordant. In this article, we consider the outcomes of�…

Purpose: We intended to elucidate the whole clinical course of Dravet syndrome (DS)
comprehensively, from infancy through adulthood. Methods: Subjects were 31 patients with�…

To describe the outcome of Dravet syndrome (DS) in adolescents and adults we conducted
a longitudinal retrospective study of two independent cohorts of 34 adolescents (group 1)�…

Dravet syndrome is one of the most severe epilepsy syndromes of early childhood, and it
comes with very high morbidity and mortality. The typical presentation is characterized by�…

Purpose: A questionnaire survey was conducted in Japan to investigate the causes and
prevalence of death related to Dravet syndrome. Methods: A questionnaire was delivered to�…

Dravet syndrome (DS) is a form of genetic refractory epilepsy. More than 80% of DS patients
carry pathogenic SCN1A mutations, and this percentage is actually higher due to false�…

Dravet syndrome is a severe infantile-onset epilepsy syndrome with a distinctive but
complex electroclinical presentation. A healthy, developmentally normal infant presents at�…

Introduction Premature mortality is a major issue in Dravet syndrome (DS). To improve
understanding of DS premature mortality, we conducted a comprehensive literature search�…

Aims of our study were to describe the early clinical features of Dravet syndrome (SMEI) and
the neurological, cognitive and behavioral outcome. The clinical history of 37 patients with�…

The aim of this study was to investigate how parents cope with and care for a child with
Dravet syndrome, a severe myoclonic epilepsy with three distinct stages. Twenty-four�…