Early onset myoclonic epilepsy and 15q26 microdeletion: Observation of the first case

Epilepsia

Volumn 50, Issue 7, 2009, Pages 1810-1815

  Veredice, Chiara ^a   Bianco, Flaviana ^a   Contaldo, Ilaria ^a   Orteschi, Daniela ^a   Stefanini, Maria Chiara ^a,b   Battaglia, Domenica ^a   Lettori, Donatella ^a   Guzzetta, Francesco ^a   Zollino, Marcella ^a  

^a CATHOLIC UNIVERSITY   (Italy)

^b IRCCS FONDAZIONE DON CARLO GNOCCHI   (Italy)

Author keywords

All epilepsy seizures; Chromosomes; Developmental disorders

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL DIAPHRAGM HERNIA; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DISEASE COURSE; FACIES; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC ANALYSIS; GROWTH RETARDATION; HUMAN; INTERSTITIAL CHROMOSOME DELETION; MENTAL DEFICIENCY; MICROARRAY ANALYSIS; MYOCLONUS EPILEPSY; ONSET AGE; PRESCHOOL CHILD; PRIORITY JOURNAL; SEIZURE; ADULT; CHROMOSOME 15; CHROMOSOME DELETION; DIAPHRAGM HERNIA; DNA MICROARRAY; EPILEPSIES, MYOCLONIC; GENETICS; HISTORY; INTELLECTUAL IMPAIRMENT; MALE; MULTIPLE MALFORMATION SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; AGE OF ONSET; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; COMPARATIVE GENOMIC HYBRIDIZATION; EPILEPSIES, MYOCLONIC; FEMALE; HERNIA, DIAPHRAGMATIC; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTELLECTUAL DISABILITY; MAGNETIC RESONANCE IMAGING; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; SYNDROME;

EID: 67649976483     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2009.02078.x     Document Type: Article

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