Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother

European Journal of Paediatric Neurology

Volumn 15, Issue 3, 2011, Pages 230-233

  Michelson, Marina ^a   Eden, Avi ^a   Vinkler, Chana ^a   Leshinsky Silver, Esther ^a,b   Kremer, Uri ^b,c   Lerman Sagie, Tally ^a,b   Lev, Dorit ^a,b  

^a WOLFSON MEDICAL CENTER   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

^c TEL AVIV SOURASKY MEDICAL CENTER   (Israel)

Author keywords

15q11 q13; Epilepsy; Schizophrenia; Supernumerary marker chromosome

Indexed keywords

ANTICONVULSIVE AGENT;

ACUTE PSYCHOSIS; ARTICLE; CASE REPORT; CHILD; CHROMOSOME; COMPARATIVE GENOMIC HYBRIDIZATION; FAMILIAL PARTIAL TRISOMY 15Q11 13; FAMILY HISTORY; FEMALE; FOURIER TRANSFORM MASS SPECTROMETRY; GENE; GENE LOCUS; HUMAN; INTELLIGENCE; INTRACTABLE EPILEPSY; KARYOTYPE; MOLECULAR CLONING; PARTIAL TRISOMY; PRIORITY JOURNAL; SCHIZOPHRENIA; SCHOOL CHILD; SEIZURE; SNRPN GENE; UBE3A GENE;

ADULT; AGE OF ONSET; ANTICONVULSANTS; CHILD; CHROMOSOMES, HUMAN, PAIR 15; DISEASE PROGRESSION; EPILEPSY; FEMALE; HUMANS; INHERITANCE PATTERNS; SCHIZOPHRENIA; TREATMENT FAILURE; TRISOMY;

EID: 79955480518     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2010.11.001     Document Type: Article

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