Eosinophilic Esophagitis (EoE) is a chronic, immune-mediated inflammatory disease of the esophagus that has rapidly transitioned from under-recognized to a major focus in gastroenterology. Driven by food allergens and characterized by eosinophilic infiltration of the esophageal lining, EoE lead

Chronic Spontaneous Urticaria (CSU) is a dermatologic condition defined by the recurrence of hives, angioedema, or both for more than six weeks, without any identifiable external trigger. Affecting approximately 0.5%–1% of the global population, CSU is more than a skin condition — it

Alpha-1 Antitrypsin Deficiency (AATD) is a rare genetic condition increasingly recognized for its role in early-onset lung and liver disease. Once confused with common COPD, AATD is now becoming a focus of targeted respiratory care, thanks to growing awareness, improved diagnostics, and evolving the

Warm Autoimmune Hemolytic Anemia (wAIHA) is a rare yet increasingly recognized hematologic disorder driven by immune system dysregulation. Once managed primarily with corticosteroids, wAIHA is now entering a new era, where precision therapies and immunomodulation are reshaping care and improving lon

Stargardt disease, a rare genetic eye disorder, is emerging as a key focus in retinal therapeutics. With no approved cure yet available, this inherited form of macular degeneration primarily affects children and young adults, progressively reducing central vision. However, advancements in gene thera