Lipid Storage Disorders are a group of rare genetic conditions that affect the body's ability to break down and store fats, known as lipids. These disorders lead to the accumulation of lipids in various tissues, which can cause damage to organs and disrupt normal bodily functions. Common types include Gaucher disease, Fabry disease, and Niemann-Pick disease. Symptoms of lipid storage disorders can vary widely but often include fatigue, pain, and organ enlargement. Diagnosis typically involves blood tests, genetic testing, and imaging studies. Treatment options may include enzyme replacement therapy, dietary changes, and supportive care to manage symptoms and improve quality of life.