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Unlocking Potential: Embracing the Future of Special Education Through Research

Unlocking Potential: Embracing the Future of Special Education Through Research

Introduction

In the ever-evolving landscape of special education, it is imperative for practitioners to stay informed about the latest research and breakthroughs that can enhance their practice. The research article titled "KMT2C/D COMPASS complex-associated diseases [KCDCOM-ADs]: an emerging class of congenital regulopathies" offers valuable insights into congenital disorders and their underlying mechanisms. By understanding these findings, educators and therapists can better support students with specific needs and contribute to their holistic development.

The Power of Research

The KMT2C/D COMPASS complexes are crucial in regulating DNA promoter and enhancer elements, which play a significant role in embryonic morphogenesis and central nervous system development. Mutations in these complexes have been linked to syndromes such as Kabuki, Rubinstein-Taybi, and Kleefstra. This research highlights the importance of understanding the genetic and molecular basis of these disorders to develop targeted interventions and therapies.

Implementing Research Outcomes

Practitioners can leverage the findings from this research in several ways:

Encouraging Further Research

While the current research provides a foundation, there is still much to learn about the KMT2C/D COMPASS complexes and their role in congenital disorders. Practitioners are encouraged to engage in further research and contribute to the growing body of knowledge. This could involve participating in research studies, collaborating with academic institutions, or pursuing advanced degrees in special education or related fields.

Conclusion

The future of special education lies in our ability to integrate cutting-edge research into everyday practice. By embracing the findings from studies like the one on KMT2C/D COMPASS complexes, we can unlock the potential of students with special needs and pave the way for a more inclusive and supportive educational environment.

To read the original research paper, please follow this link: KMT2C/D COMPASS complex-associated diseases [KCDCOM-ADs]: an emerging class of congenital regulopathies.


Citation: Lavery, W. J., Barski, A., Wiley, S., Schorry, E. K., & Lindsley, A. W. (2020). KMT2C/D COMPASS complex-associated diseases [KCDCOM-ADs]: an emerging class of congenital regulopathies. Clinical Epigenetics, 12(1), 10.1186/s13148-019-0802-2.
Marnee Brick, President, TinyEYE Therapy Services

Author's Note: Marnee Brick, TinyEYE President, and her team collaborate to create our blogs. They share their insights and expertise in the field of Speech-Language Pathology, Online Therapy Services and Academic Research.

Connect with Marnee on LinkedIn to stay updated on the latest in Speech-Language Pathology and Online Therapy Services.

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