Title Genomo persitvarkymai, esant įgimtiems centrinės nervų sistemos raidos sutrikimams: kilmė, genominiai mechanizmai, funkcinės ir klinikinės pasekmės. Darbų apžvalga /
Translation of Title Genome rearrangements in neurodevelopmental disorders of the central nervous system: origins, genomic mechanisms, functional and clinical consequences. Review article.
Authors Kučinskas, Vaidutis ; Preikšaitienė, Eglė ; Ambrozaitytė, Laima ; Cimbalistienė, Loreta ; Utkus, Algirdas
DOI 10.15388/NS.2022.26.3
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Is Part of Neurologijos seminarai.. Vilnius : Rotas. 2022, t. 26, Nr. 1, p. 15-26.. ISSN 1392-3064. eISSN 2424-5917
Keywords [eng] genome rearrangements ; congenital developmental disorders ; intellectual disability ; Alkuraya-Kucinskas syndrome
Abstract [eng] Intellectual disability affects about 1-2% of the general population worldwide, and this is the leading socio-economic problem of the healthcare system. Reasearch into the genetic causes of intellectual disability is challenging because these conditions are genetically heterogeneous with many different genetic alterations resulting in clinically indistinguishable phenotypes. Extensive molecular technologies are being used in research to determine the genetic causes of these conditions. In our research, the detection of chromosomal aberrations by molecular karyotyping and whole exome sequencing capable of uncovering pathogenic variants in any of the human genes were the main technologies used to identify the molecular causes of intellectual disability. Collaboration with foreign scientific institutions for further clinical, molecular and functional investigations of rare causes of intellectual disability has allowed the characterisation of rare known and new syndromes. We believe that new insights into the molecular causes and pathogenesis mechanisms of the intellectual disability may be useful in developing treatment options in the future.
Published Vilnius : Rotas
Type Journal article
Language Lithuanian
Publication date 2022
CC license CC license description