Autonomic seizures versus syncope in 18q- deletion syndrome: A case report

Epilepsia

Volumn 41, Issue 8, 2000, Pages 1039-1043

  Sturm, Kerstin ^a   Knake, Susanne ^a   Schomburg, Ulrich ^a   Wakat, Jörg P ^a   Hamer, Hajo M ^a   Fritz, Barbara ^a   Oertel, Wolfgang H ^a   Rosenow, Felix ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

Automated seizure detection; Chromosome 18; Dysmyelination; Ictal tachycardia; Myelin basic protein

Indexed keywords

CARBAMAZEPINE; MYELIN BASIC PROTEIN;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 18Q; CHROMOSOME ANALYSIS; DIAGNOSTIC VALUE; DISEASE ASSOCIATION; ELECTROENCEPHALOGRAM; EPILEPSY; GENE DELETION; GENETIC DISORDER; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SEIZURE; SYNCOPE;

EID: 0033869328     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1528-1157.2000.tb00291.x     Document Type: Article

References (13)

1. Clinical and chromosomal studies of the 18q- syndrome
2. Neurologic manifestations in 18q- syndrome
3. Growth hormone insufficiency associated with haploinsufficiency at 18q23
4. Partial epileptic seizures of different origin variably effect cardiac rhythm
5. Some autonomic concomitants of ictal automatisms: A study of temporal lobe attacks
6. Autonomic signs associated with seizures
7. Semiological seizure classification
8. Recognizing syncope: Pitfalls and surprises
9. The brain in the 18q-syndrome
10. Heart rate signal artifact identification improves tachycardiograph seizure detection
11. Combined EEG and EKG detection algorithms improve computerized seizure identification
12. White matter changes associated with deletions of the long arm of chromosome 18: A dysmyelinating disorder?
13. MR findings in the central nervous system of patients with a deletion of the long arm of chromosome 18 (18q-)