Epidermolysis Bullosa: Understanding the Rare Skin Disorder (EB)
Epidermolysis Bullosa, commonly abbreviated as EB, is a group of rare genetic conditions that affect the skin and mucous membranes….
Ehlers-Danlos Syndrome: A Complete Guide to Symptoms, Types, and Management
Ehlers-Danlos Syndrome, often abbreviated as EDS, is a group of inherited disorders that primarily affect the connective tissues in the…
Edwards Syndrome (Trisomy 18): Overview, Causes, Symptoms & Care
Edwards Syndrome, also known as Trisomy 18, is a rare but serious genetic condition that affects the development of a…
Dwarfism: Types, Causes, and Daily Life Challenges
Dwarfism, a medical condition characterized by short stature, affects individuals in various ways. People with this condition often face unique…
Duchenne Muscular Dystrophy: Causes, Symptoms, Progression, and Care Options
Duchenne Muscular Dystrophy, commonly abbreviated as DMD, is a rare genetic disorder that primarily affects males. It leads to progressive…
Down Syndrome: Causes, Features, and Support
Down Syndrome, often abbreviated as DS, is a genetic condition that affects individuals worldwide. It is one of the most…
DiGeorge Syndrome (22q11.2 Deletion Syndrome): Overview, Symptoms, and Care
DiGeorge Syndrome, also known as 22q11.2 Deletion Syndrome, is a genetic disorder caused by the deletion of a small segment…
Cystic Fibrosis: Understanding the Disease, Symptoms, and Treatments
Cystic fibrosis, often abbreviated as CF, is a chronic and life-threatening genetic disorder that affects multiple systems in the body….
Craniosynostosis: A Detailed Overview of Premature Skull Fusion
Craniosynostosis, often abbreviated as CS, is a medical condition characterized by the premature fusion of one or more sutures in…
Congenital Adrenal Hyperplasia (CAH): Overview, Causes, Symptoms, and Treatments
Congenital Adrenal Hyperplasia, commonly abbreviated as CAH, is a group of inherited genetic disorders that affect the adrenal glands. These…