A case of startle epilepsy associated with IL1RAPL1 gene deletion

Pediatric Neurology

Volumn 51, Issue 2, 2014, Pages 271-274

  Dinopoulos, Argiris ^a   Stefanou, Maria Ioanna ^b   Attilakos, Achilleas ^a   Tsirouda, Maria ^a   Papaevangelou, Vassiliki ^a  

^a NATIONAL AND KAPODISTRIAN UNIVERSITY OF ATHENS   (Greece)

^b KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

adrenocorticotropic hormone; atonic episodes; mental retardation; startle syndromes; startle induced seizures

Indexed keywords

ANTICONVULSIVE AGENT; CLONAZEPAM; GLYCOPROTEIN; TETRACOSACTIDE; TOPIRAMATE; VIGABATRIN; IL1RAPL1 PROTEIN, HUMAN; INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN;

AMNIOCENTESIS; ANTICONVULSANT THERAPY; ARTICLE; AUDITORY BRAIN STEM IMPLANT; BRAIN DISEASE; CASE REPORT; CESAREAN SECTION; CHILD; CHROMOSOME XP; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISORDER; DROP ATTACK; DRUG DOSE REDUCTION; ELECTROENCEPHALOGRAPHY; GENE; GENE DELETION; GENE LOCUS; GENETIC DISORDER; HUMAN; INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN LIKE 1 GENE; MALE; MENTAL DEFICIENCY; MUSCLE HYPERTONIA; MUSCLE HYPOTONIA; NERVE CELL DIFFERENTIATION; NEUROLOGIC EXAMINATION; NEUROPHYSIOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOGENESIS; PRESCHOOL CHILD; PRIORITY JOURNAL; SEIZURE; STARTLE EPILEPSY; STIMULUS RESPONSE; SYNAPSE; TREATMENT RESPONSE; FAINTNESS; GENETICS; INFANT; REFLEX EPILEPSY; STARTLE REFLEX;

DEVELOPMENTAL DISABILITIES; EPILEPSY, REFLEX; GENE DELETION; HUMANS; INFANT; INTERLEUKIN-1 RECEPTOR ACCESSORY PROTEIN; MALE; REFLEX, STARTLE; SYNCOPE;

EID: 84904870637     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2014.04.011     Document Type: Article

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