Open AccessRing chromosome 20: A further contribution to the delineation of epileptic phenotype
Author(s) -
Milan Borković,
Goran Čuturilo,
Nataša Cerovac
Publication year - 2022
Publication title -
vojnosanitetski pregled
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.123
H-Index - 19
eISSN - 2406-0720
pISSN - 0042-8450
DOI - 10.2298/vsp200601096b
Subject(s) - epilepsy , semiology , status epilepticus , medicine , ring chromosome , pediatrics , abnormality , epilepsy syndromes , magnetic resonance imaging , neuroimaging , cognition , chromosome , neuroscience , karyotype , psychology , psychiatry , genetics , biology , radiology , gene
. Ring chromosome 20 [r(20)] syndrome is a rare genetic abnormality where two arms of the 20th chromosome fuse forming a ring chromosome, resulting in intractable epilepsy and wide range of behavioral problems and cognitive deficits. Case report. We presented four patients with r (20) syndrome diagnosed between the years 2000?2018. In all patients we analyzed clinical epilepsy features (seizure semiology, seizure frequency/drug response, the presence of nonconvulsive status epilepticus), cognitive status and the phenotype characteristics. The average age of epilepsy onset was 6 years. All four patients had nocturnal epileptic events and normal brain magnetic resonance (MR) imaging. Dysmorphism was present in two children, behavioral problems also in two children and intellectual disabilities were observed in three children. R(20) syndrome mosaicism ranged between 17% and 83% of blood lymphocytes. Conclusion. Despite the small size of our group, we think that our findings have clinical relevance. Refractory child-hood onset epilepsy and especially the occurrence of nocturnal epileptic events should help physicians to recognize this chromosomopathy. Routine karyotyping can be employed to identify the patients easily.