Ulcerative colitis (UC) is a chronic inflammatory bowel disease (IBD) that causes inflammation and ulcers in the digestive tract, primarily affecting the colon and rectum. It can significantly impact the quality of life due to its unpredictable flare-ups and persistent symptoms. This blog provides an in-depth look at ulcerative colitis, its symptoms, treatments, and ways…
Genetic testing has revolutionized the way we understand inherited diseases, helping individuals and families make informed health decisions. Whether you’re looking for answers to conditions like hypertrophic cardiomyopathy, familial hypercholesterolemia, or genetic liver diseases, genetic screening serves as a cornerstone of modern healthcare. This guide explores genetic screening for various conditions, its benefits, limitations, and…
Myasthenia Gravis (MG) is a chronic autoimmune disorder that weakens skeletal muscles, impacting activities like breathing, swallowing, and walking. While there is no specific diet to cure MG, proper nutrition plays a vital role in managing symptoms, supporting overall health, and improving quality of life. This blog explores the relationship between nutrition and Myasthenia Gravis,…
Beta thalassemia is an inherited blood disorder that reduces the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. This condition can range from mild (β thalassemia minor) to severe (beta thalassemia major). Recent advancements in gene therapy, including the FDA-approved Zynteglo by Bluebird Bio, offer promising treatment options…
Duchenne Muscular Dystrophy (DMD) is a severe genetic disorder that primarily affects muscles, leading to progressive muscle degeneration and weakness. It is one of the most common types of muscular dystrophy, with significant advancements in gene therapy offering hope for affected individuals and their families. This blog delves into the nature of DMD, its inheritance…