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The sixth international RASopathies symposium: Precision medicine-From promise to practice
Karen W Gripp1, Lisa Schill2, Lisa Schoyer2
1Al duPont Hospital for Children, Wilmington, Delaware.
American Journal of Medical Genetics. Part A
|December 12, 2019
Summary
RASopathies are genetic disorders caused by RAS-mitogen activated protein kinase (MAPK) pathway gene variants. The Sixth International RASopathies Symposium explored precision medicine strategies and drug development for these complex conditions.
Area of Science:
- Genetics
- Molecular Biology
- Medical Science
Background:
- RASopathies are a group of genetic disorders stemming from germline pathogenic variants in RAS-mitogen activated protein kinase (MAPK) pathway genes.
- These disorders are characterized by RAS/MAPK pathway dysregulation, leading to shared phenotypic manifestations across multiple organ systems.
- The lifelong and potentially life-limiting medical complications associated with RASopathies highlight the need for advanced treatment strategies.
Framework:
- The Sixth International RASopathies Symposium convened experts to focus on precision medicine approaches for RASopathies.
- Attendees included basic scientists, clinicians, patient advocates, and pharmaceutical and governmental representatives.
- Discussions centered on novel RASopathy genes, variants, and animal models relevant to therapeutic development.
Implementation:
- The symposium explored current medication trials and drug development pipelines for RASopathies.
- Key discussions involved establishing and measuring meaningful endpoints for clinical treatment trials.
- Strategies for ensuring drug availability to patients post-trial completion were also addressed.
Implications:
- Advancements in understanding RASopathies and their genetic underpinnings are paving the way for targeted therapies.
- Precision medicine holds significant promise for improving outcomes and managing complications in patients with RASopathies.
- Collaborative efforts among researchers, clinicians, and industry stakeholders are crucial for accelerating drug development and patient access.
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