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…
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…
Mitochondrial disorders are a group of rare and complex conditions resulting from dysfunctional mitochondria, often referred to as the powerhouses of cells. These organelles are vital for producing energy that supports various bodily functions. When they fail, they cause significant health challenges. Consequently, individuals with mitochondrial disorders often face diverse symptoms that affect multiple organ…
Neurofibromatosis (NF) is a genetic disorder that affects the nervous system and causes tumors to grow along nerves. These tumors are generally benign but can sometimes cause complications, depending on their size and location. There are three main types of neurofibromatosis: NF1, NF2, and schwannomatosis. This blog explores the causes, symptoms, and treatment options for…
Hyperthyroidism, often referred to as an overactive thyroid, occurs when the thyroid gland produces excessive thyroid hormones. This condition can significantly impact metabolism, heart rate, and overall energy levels. In this blog, we will explore the symptoms, diagnosis, and treatment options for Overactive Thyroid, including subclinical Thyroid Hyperactivity. What is Hyperthyroidism? Thyroid Hyperactivity is a…