Topic: Screening and Treatment of Barth Syndrome

Barth Syndrome, a rare and complex genetic disorder, poses unique challenges in its screening and treatment. As the medical community strives for a deeper understanding of this condition, there is an urgent need for cutting-edge research and innovative approaches to enhance screening methods and refine treatment protocols. This Special Issue aims to bring together experts in the field to explore and contribute to the latest advancements in the screening and treatment of Barth Syndrome. We welcome contributions that delve into novel diagnostic techniques, therapeutic interventions, and multidisciplinary strategies, fostering a collaborative effort to improve outcomes for individuals affected by Barth Syndrome. We invite you to join us in addressing this critical topic and shaping the future of Barth Syndrome research and care.

29 Nov 2024