Williams Syndrome: A Genetic Disorder Explained
Williams Syndrome, often abbreviated as WS, is a rare genetic condition that affects approximately one in every ten thousand people…
Von Willebrand Disease: Causes, Symptoms, and Treatments
Von Willebrand Disease, commonly abbreviated as VWD, is a genetic disorder that affects the blood’s ability to clot properly. It…
Tuberous Sclerosis: A Detailed Overview of Symptoms, Diagnosis, and Treatments
Tuberous Sclerosis Complex (TSC) is a rare genetic disorder that affects multiple systems in the body. It causes non-cancerous tumors…
Turner Syndrome: A Complete Overview of Symptoms, Diagnosis, and Treatment
Turner Syndrome, often abbreviated as TS, is a rare chromosomal condition that affects females. It occurs when one of the…
Triple X Syndrome (Trisomy X): A Complete Overview
Triple X Syndrome, also known as Trisomy X, is a chromosomal condition that affects females. It occurs when a female…
Treacher Collins Syndrome: A Detailed Overview of Facial Bone Development Disorder (TCS)
Treacher Collins Syndrome, commonly abbreviated as TCS, is a rare genetic condition that affects the development of facial bones and…
Thalassemia: Types, Causes, Symptoms, and Treatments
Thalassemia, often abbreviated as THAL, is a group of inherited blood disorders that affect the production of hemoglobin, the protein…
Tay-Sachs Disease: Understanding the Genetic Disorder
Tay-Sachs Disease, often abbreviated as TSD, is a rare and devastating genetic condition that primarily affects infants and young children….
Stickler Syndrome: A Comprehensive Overview
Stickler Syndrome, often abbreviated as SS, is a rare genetic disorder that affects multiple systems in the body, primarily targeting…
Spinal Muscular Atrophy (SMA): Overview, Types, Symptoms & Care
Spinal Muscular Atrophy, commonly abbreviated as SMA, is a rare genetic disorder that affects the nervous system and leads to…