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. 2023 Jan 23;14(2):299.
doi: 10.3390/genes14020299.

Status Epilepticus in Chromosomal Disorders Associated with Epilepsy: A Systematic Review

Affiliations

Status Epilepticus in Chromosomal Disorders Associated with Epilepsy: A Systematic Review

Luca Bergonzini et al. Genes (Basel). .

Abstract

Status Epilepticus (SE) is a neurological emergency resulting from the failure of mechanisms of seizure termination or from the initiation of mechanisms that lead to prolonged seizures. The International League Against Epilepsy (ILAE) identified 13 chromosomal disorders associated with epilepsy (CDAE); data regarding SE occurrence in these patients is lacking. A systematic scoping review was conducted to outline current literature evidence about clinical features, treatments, and outcomes of SE in pediatric and adult patients with CDAE. A total of 373 studies were identified with the initial search; 65 of these were selected and regarded as SE in Angelman Syndrome (AS, n = 20), Ring 20 Syndrome (R20, n = 24), and other syndromes (n = 21). Non-convulsive status epilepticus (NCSE) is frequently observed in AS and R20. No specific, targeted therapies for SE in CDAE are available to date; anecdotal reports about SE treatment are described in the text, as well as various brief- and long-term outcomes. Further evidence is needed to precisely portray the clinical features, treatment options, and outcomes of SE in these patients.

Keywords: Angelman Syndrome; Ring 20 Syndrome; Status Epilepticus; anti-seizure medications; chromosomal disorders; epilepsy.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
PRISMA flow chart.

References

    1. Trinka E., Cock H., Hesdorffer D., Rossetti A.O., Scheffer I.E., Shinnar S., Shorvon S., Lowenstein D.H. A definition and classification of status epilepticus—Report of the ILAE Task Force on Classification of Status Epilepticus. Epilepsia. 2015;56:1515–1523. doi: 10.1111/epi.13121. - DOI - PubMed
    1. Wylie T., Sandhu D.S., Murr N. StatPearls. StatPearls Publishing; Treasure Island, FL, USA: 2022. [(accessed on 20 December 2022)]. Status Epilepticus. Available online: http://www.ncbi.nlm.nih.gov/books/NBK430686/ - PubMed
    1. Sankar R., Shin D.H., Liu H., Mazarati A., De Vasconcelos A.P., Wasterlain C.G. Patterns of Status Epilepticus-Induced Neuronal Injury during Development and Long-Term Consequences. J. Neurosci. 1998;18:8382–8393. doi: 10.1523/JNEUROSCI.18-20-08382.1998. - DOI - PMC - PubMed
    1. Chin R.F.M. The outcomes of childhood convulsive status epilepticus. Epilepsy Behav. 2019;101 Pt B:106286. doi: 10.1016/j.yebeh.2019.04.039. - DOI - PubMed
    1. Smith D.M., McGinnis E.L., Walleigh D.J., Abend N.S. Management of Status Epilepticus in Children. J. Clin. Med. 2016;5:47. doi: 10.3390/jcm5040047. - DOI - PMC - PubMed

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