Welcome Message

Saturday, October 3, 2026 | LAU Beirut Campus – Irwin Hall Auditorium
8:30 AM–12:30 PM

We invite you to participate in “Early Detection Matters: Newborn Screening for Rare Diseases,” a scientific and awareness symposium organized by the Department of Human Genetics, LAU Gilbert and Rose-Marie Chagoury School of Medicine, in collaboration with SESOBEL, AFM, and Myo-SF.

This symposium aims to raise awareness about the importance of early detection and newborn screening for rare diseases, particularly conditions in which timely diagnosis and intervention can significantly improve health outcomes and quality of life. Through expert presentations and discussion, participants will describe current approaches to newborn screening, identify the clinical benefits and challenges associated with early detection of rare and neuromuscular disorders, discuss advances in diagnosis and treatment, and apply appropriate approaches to communicating a diagnosis with patients and families.

The symposium will provide an opportunity for healthcare professionals, researchers, patient organizations, and other stakeholders to exchange knowledge and explore the current status and future perspectives of newborn screening in Lebanon and beyond.

The target audience includes healthcare professionals, faculty, medical students, residents, researchers, and healthcare providers involved in the care of individuals with rare and neuromuscular diseases, including physiotherapists, occupational therapists, psychologists, nurses, and pharmacists. Representatives of patient organizations, specialized institutions, and other stakeholders interested in rare diseases and newborn screening are also welcome to participate.

We look forward to welcoming you to this important symposium and to fostering meaningful dialogue on how early detection, timely diagnosis, and access to appropriate care can make a difference in the lives of individuals and families affected by rare diseases.

With our warm regards,

Andre Megarbane, MD, PhD
Activity Director
Chair, Department of Human Genetics
LAU Gilbert and Rose-Marie Chagoury School of Medicine