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Striano. J Transl Genet Genom 2024;8:278-80 Journal of Translational
DOI: 10.20517/jtgg.2024.40
Genetics and Genomics

Editorial Open Access

Unraveling the genetic tapestry of
neurodevelopmental disorders: a new horizon

Pasquale Striano 1,2
1
Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa 16147, Italy.
2
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova,
Genoa 16147, Italy.
Correspondence to: Prof. Pasquale Striano, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal
and Child Health, University of Genoa, Genoa 16147, Italy; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto
Giannina Gaslini, Via Gerolamo Gaslini 5, Genoa 16147, Italy. E-mail: pstriano@unige.it

How to cite this article: Striano P. Unraveling the genetic tapestry of neurodevelopmental disorders: a new horizon. J Transl Genet
Genom 2024;8:278-80. https://dx.doi.org/10.20517/jtgg.2024.40

Received: 26 Jul 2024 Accepted: 14 Aug 2024 Published: 16 Aug 2024

Academic Editor: Sanjay Gupta Copy Editor: Fangling Lan Production Editor: Fangling Lan

In the realm of neurodevelopmental disorders, the confluence of genetics and neurology heralds a
promising frontier for understanding and treating conditions that have long eluded definitive elucidation.
This Special Issue on “Genetic Neurodevelopmental Diseases” encapsulates a pivotal moment in this
journey, showcasing pioneering research that bridges the gap between genetic anomalies and clinical
manifestations. As we delve into the complexities of these disorders, the contributions within this issue not
only illuminate the intricate genetic underpinnings but also pave the way for innovative therapeutic
strategies, underscoring the transformative potential of genetic research in neurodevelopmental science.

The first article by Aledo-Serrano et al. thrusts us into the enigmatic world of developmental and epileptic
encephalopathies (DEEs), challenging us to reconsider our approach when genetic testing falls short of
providing answers . This work underscores the imperative for continuous genetic reevaluation and the
[1]
embracing of novel diagnostic paradigms, setting a tone of resilience and innovation that resonates
throughout this issue.

© The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0
International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing,
adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as
long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and
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