KUWAIT, Sept 11: Dr. Laila Bastaki, Head of the Genetic Diseases Center at the Ministry of Health, emphasized the importance of incorporating genetic testing for Duchenne muscular dystrophy (DMD) into newborn screenings. This approach would enable early treatment, leading to better outcomes and reduced severity of disability.

In an interview with KUNA during the World Awareness Day for DMD, held in collaboration with the Ministry of Foreign Affairs, Dr. Bastaki highlighted the need for a society that offers equal opportunities for DMD patients. She also stressed the importance of educating medical professionals and patients' families about diagnosis and treatment through media channels.

Dr. Bastaki recommended establishing a Duchenne Muscular Dystrophy Association to facilitate the exchange of experiences and information between patients' families and specialists. This association would support patients and provide integrated clinics to deliver comprehensive services without long wait times. (KUNA)