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Striano. J Transl Genet Genom 2024;8:278-80  https://dx.doi.org/10.20517/jtgg.2024.40  Page 280

               nuanced genetic architecture of these conditions. Integrating research findings into clinical practice will
               enhance personalized medicine approaches, ensuring that treatment strategies are tailored to the
               individual's genetic profile. The exploration of environmental and epigenetic factors will also be vital in
               comprehending the full scope of these disorders.


               In conclusion, this Special Issue is not an endpoint but a beacon, guiding us toward a future where the
               mysteries of genetic neurodevelopmental diseases are unraveled, and the lives of those affected are
               profoundly improved. Let us carry forward the torch of inquiry, collaboration, and compassion that has
               been so vividly ignited within these pages.

               DECLARATIONS
               Authors’ contributions
               The author contributed solely to the article.

               Availability of data and materials
               Not applicable.


               Financial support and sponsorship
               None.


               Conflicts of interest
               The author declared that there are no conflicts of interest.


               Ethical approval and consent to participate
               Not applicable.


               Consent for publication
               Not applicable.


               Copyright
               © The Author(s) 2024.

               REFERENCES
               1.      Aledo-Serrano A, Sánchez-Alcudia R, Toledano R, et al. Developmental and epileptic encephalopathies after negative or inconclusive
                  genetic testing: what is next? J Transl Genet Genom 2021;5:443-55.  DOI
               2.      Lyulcheva-Bennett E, Blumenow W, O’Connor A, Kelly M, Bennett D, Fattah A. Towards an understanding of the aetiology, genomic
                  landscape and management of Moebius syndrome. J Transl Genet Genom 2023;7:259-73.  DOI
               3.      Bone M, Goodspeed K, Sirsi D. Epilepsy and electroencephalography in Pitt-Hopkins syndrome. J Transl Genet Genom 2022;6:169-78.
                  DOI
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