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18 Possible Causes for 3-4 Hz Spikes, Genetic Heterogeneity, Paroxysmal Activity - Spikes Occipital Left

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  • Benign Adult Familial Myoclonic Epilepsy

    Abstract Benign adult familial myoclonic epilepsy (BAFME) has been mapped to chromosome 8q24; however, genetic heterogeneity has been recently suggested.[ncbi.nlm.nih.gov] Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.[reference.medscape.com] This observation would confirm that BAFME is a worldwide, genetically heterogeneous condition, probably with Japanese families linked to 8q24 and European families to 2p11.1[ncbi.nlm.nih.gov]

  • Juvenile Myoclonic Epilepsy

    Abstract Juvenile myoclonic epilepsy (JME) is a clinically and genetically heterogenous, generalized epilepsy syndrome usually starting in adolescence.[ncbi.nlm.nih.gov] Interictal electroencephalography (EEG) in JME shows interictal epileptiform discharges such as generalized spikes, polyspikes, bilateral-synchronous 4-6/s spike-wave complexes[go.galegroup.com] BACKGROUND: Juvenile myoclonic epilepsy (JME), is an early-onset inherited generalized epilepsy which displays genetic heterogeneity, with at least 10 known loci.[ncbi.nlm.nih.gov]

  • Epilepsy

    Progressive myoclonic epilepsies (PME) are a clinically and genetically heterogeneous group of rare diseases characterized by myoclonic seizures, tonic-clonic seizures, and[ncbi.nlm.nih.gov] […] to 8 years of age, in an otherwise apparently healthy child. 3 The classic electroencephalogram (EEG) shows generalized spike-wave bursts (of 3 Hz) with normal background[doi.org] This observation along with our previous findings of hot water genetic loci at 10q21.3-q22.3 (OMIM: 613339) and 4q24-q28 (OMIM: 613340), indicates unanticipated genetic heterogeneity[ncbi.nlm.nih.gov]

  • Idiopathic Generalized Epilepsy

    The lack of significant association evidence of single variants with disease in this two-stage approach emphasizes the high genetic heterogeneity of epilepsy disorders, suggests[ncbi.nlm.nih.gov] 4 Hz spikes and waves in all regions of the brain 1 st -line : valproic acid Avoid triggers : sleep deprivation, alcohol, drugs, flickering lights 60% are seizure -free under[amboss.com] […] etiology, where heterogeneous combinations of genetic factors determine the disease phenotype.[ncbi.nlm.nih.gov]

  • Myoclonic-Astatic Epilepsy

    […] influences and clues for genetic heterogeneity, and discuss strategies that may be helpful in elucidating the etiology of MAE in light of current genetic techniques.[ncbi.nlm.nih.gov] […] presence of generalized spike- or polyspike-wave EEG discharges at 2-3 Hz, without focal spike discharges; and (4) exclusion of severe and benign myoclonic epilepsy (SME,[ncbi.nlm.nih.gov] Doose Syndrome is likely to be genetically heterogeneous and – in contrast to Dravet Syndrome – caused by various different genes.[epilepsygenetics.net]

  • Generalized Clonic or Tonic-Clonic Seizures

    Genetic Heterogeneity of Progressive Myoclonic EpilepsyProgressive myoclonic epilepsy refers to a clinically and genetically heterogeneous group of neurodegenerative disorders[mendelian.co] The EEG shows generalised spike and wave discharges of 3 to 4 Hz and some with photic sensitivity. This is potentially a lifelong epilepsy.[pennsw.com.au] Genetic Heterogeneity of Mosaic Variegated Aneuploidy SyndromeSee also MVA2 ( OMIM ), caused by mutation in the CEP57 gene ( OMIM ) on chromosome 11q21, and MVA3 ( OMIM ),[mendelian.co]

  • West Syndrome

    West syndrome is genetically heterogeneous, and its genetic causes have not been fully elucidated.[ncbi.nlm.nih.gov] This disorder is genetically heterogeneous, with up to a fifth of cases resulting from mutations in the CDKL5 gene.[genedx.com] Despite the heterogeneity of unexplained West syndrome, the combination of array CGH and whole-exome sequencing is an effective means of evaluating the genetic background[ncbi.nlm.nih.gov]

  • Juvenile Absence Epilepsy

    Página 112 - JC (1998) Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24. Am. J. Hum.[books.google.es] Diagnostic methods Diagnosis relies on the clinical features and on electroencephalogram (EEG) recorded awake and during sleep, that displays a generalized 3-4 Hz spike-and-slow-wave[orpha.net] Generalized 3-4 Hz spike or polyspike slow-wave complexes. Neuro Imaging: Not usually required. Mainly from other IGEs such as CAE or Juvenile Myoclonic Epilepsy (JME).[pennsw.com.au]

  • Encephalopathy

    SUMMARY: Neonatal encephalopathy is a heterogeneous disorder that is characterized by alterations in mental status, hypotonia, seizures, and abnormalities in feeding and respiration[ncbi.nlm.nih.gov] Posterior reversible encephalopathy syndrome (PRES) is a rare neurologic condition that manifests with heterogeneous clinical findings, including altered mental status, seizure[ncbi.nlm.nih.gov] LESSONS: HE may cause highly heterogeneous clinical features, particularly MRI findings.[ncbi.nlm.nih.gov]

  • Uremic Encephalopathy

    heterogeneous disease that may exist in both autosomal dominant and recessive forms.[jnnp.bmj.com] 2 Cambridge screening protocol for von Hippel-Lindau disease in affected patients and at risk relatives 1 POLYCYSTIC KIDNEY DISEASE Polycystic kidney disease (PCKD) is a genetically[jnnp.bmj.com] More recently, a reversible posterior leukoencephalopathy syndrome has been described in a heterogeneous group of patients, including those undergoing renal, liver, and bone[jnnp.bmj.com]

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