TY - JOUR
T1 - Disorders of early language development in Dravet syndrome
AU - Chieffo, Daniela Pia Rosaria
AU - Battaglia, Domenica Immacolata
AU - Lucibello, Simona
AU - Gambardella, Maria Luigia
AU - Moriconi, Federica
AU - Ferrantini, Gloria
AU - Leo, Giuseppina
AU - Dravet, Charlotte
AU - Mercuri, Eugenio Maria
AU - Guzzetta, Francesco
PY - 2016
Y1 - 2016
N2 - The aim of this study was to investigate language disorders prospectively in patients with Dravet syndrome (DS) during the first years of life in order to identify their features and possibly the underlying mechanisms of the disease. At the Child Neurology Unit of Catholic University in Rome (Italy), thirteen patients with typical findings of DS were enrolled in the study. Full clinical observations, including neurological examination and long-term EEG monitoring, were prospectively and serially performed until a mean of 6 years of age (range: 4 years to 7 years and 8 months). The epileptic history was also collected in each case. In particular, developmental, cognitive, and detailed language assessments were performed with different tests according to the age of the patient.In addition to cognitive decline, characteristic language impairment was also found with a relative preservation of receptive abilities (comprehension) and a strong impairment of productive skills. This defect in sensorimotor verbal processing integration is discussed to highlight the possible mechanisms underlying cognitive decline.
AB - The aim of this study was to investigate language disorders prospectively in patients with Dravet syndrome (DS) during the first years of life in order to identify their features and possibly the underlying mechanisms of the disease. At the Child Neurology Unit of Catholic University in Rome (Italy), thirteen patients with typical findings of DS were enrolled in the study. Full clinical observations, including neurological examination and long-term EEG monitoring, were prospectively and serially performed until a mean of 6 years of age (range: 4 years to 7 years and 8 months). The epileptic history was also collected in each case. In particular, developmental, cognitive, and detailed language assessments were performed with different tests according to the age of the patient.In addition to cognitive decline, characteristic language impairment was also found with a relative preservation of receptive abilities (comprehension) and a strong impairment of productive skills. This defect in sensorimotor verbal processing integration is discussed to highlight the possible mechanisms underlying cognitive decline.
KW - Behavioral Neuroscience
KW - Child
KW - Child, Preschool
KW - Cognition Disorders
KW - Cognitive decline
KW - Comprehension
KW - Dravet syndrome
KW - Electroencephalography
KW - Epilepsies, Myoclonic
KW - Female
KW - Humans
KW - Language Development
KW - Language Development Disorders
KW - Language developmental disorders
KW - Male
KW - Neurologic Examination
KW - Neurology
KW - Neurology (clinical)
KW - Neuropsychological Tests
KW - Behavioral Neuroscience
KW - Child
KW - Child, Preschool
KW - Cognition Disorders
KW - Cognitive decline
KW - Comprehension
KW - Dravet syndrome
KW - Electroencephalography
KW - Epilepsies, Myoclonic
KW - Female
KW - Humans
KW - Language Development
KW - Language Development Disorders
KW - Language developmental disorders
KW - Male
KW - Neurologic Examination
KW - Neurology
KW - Neurology (clinical)
KW - Neuropsychological Tests
UR - http://hdl.handle.net/10807/95346
UR - http://www.elsevier.com/inca/publications/store/6/2/2/8/2/2/index.htt
U2 - 10.1016/j.yebeh.2015.10.027
DO - 10.1016/j.yebeh.2015.10.027
M3 - Article
SN - 1525-5050
VL - 54
SP - 30
EP - 33
JO - EPILEPSY & BEHAVIOR
JF - EPILEPSY & BEHAVIOR
ER -