A pioneering gene therapy has shown promising results in restoring sight in young children with AIPL1-associated severe retinal dystrophy—an ultra-rare genetic condition that causes profound sight impairment from birth and, until now, had no existing treatment. The findings, published in The Lancet, mark a major step forward in tackling inherited blindness.
This episode explores the inspiring work of Orbis International, a nonprofit preventing blindness and restoring sight in underserved communities. Dr Maria Berrocal, Associate Professor and Orbis Volunteer Faculty, shares her experience aboard the Orbis Flying Eye Hospital, a fully equipped surgical and teaching hospital on an aircraft, and discusses the importance of global collaboration in building sustainable, high-quality eye care systems around the world.
In this letter, Mr Wagih Aclimandos, President of the European Society of Ophthalmology (SOE) and Consultant Ophthalmic Surgeon and Lead Clinician for Paediatric Ophthalmology and Strabismus Services at King’s College Hospital, London, shares his insights and highlights of what ...
The International Congenital Corneal Opacification Network (ICCON) is a pioneering initiative dedicated to improving the care and management of children with congenital corneal opacities worldwide. Established by the World Society of Paediatric Ophthalmology and Strabismus (WSPOS) in collaboration with the Paediatric Keratoplasty Association (PKA), ICCON aims to connect specialists, surgeons, and healthcare professionals with a shared mission: ensuring that children with these rare yet challenging conditions receive the expertise and treatment they need.
In this Q&A for touchOPHTHALMOLOGY’ Future Leaders 2025 series, Dr Alió del Barrio reflects on the key mentors who shaped his career, shares his insights on balancing clinical practice with research and personal life and offers invaluable advice to rising stars in the field.
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