Hereditary Hemorrhagic Telangiectasia (HHT): Overview, Causes, Symptoms & Care
Hereditary Hemorrhagic Telangiectasia, commonly abbreviated as HHT, is a rare genetic disorder that affects blood vessels throughout the body. This…
Hemophilia: Understanding the Bleeding Disorder (Factor VIII Deficiency)
Hemophilia, often abbreviated as Hemo, is a rare genetic disorder that affects the body’s ability to form blood clots. This…
Iron Overload Disorder (Hemochromatosis): Causes, Symptoms, Diagnosis & Management
Iron overload disorder, commonly referred to as hemochromatosis, is a medical condition characterized by excessive accumulation of iron in the…
Gaucher’s Disease (Disorder of Fat Storage): Overview, Types, Symptoms & Care
Gaucher’s Disease, often abbreviated as GD, is a rare genetic disorder that affects the body’s ability to break down a…
Fragile X Syndrome (FXS): Causes, Symptoms & Care
Fragile X Syndrome, often abbreviated as FXS, is a genetic condition that causes intellectual and developmental challenges. It is the…
Floppy Baby Syndrome (Hypotonia): Overview, Causes, and Care
Floppy Baby Syndrome, also known as Hypotonia, is a condition characterized by decreased muscle tone in infants. The term “floppy”…
Fetal Alcohol Syndrome: Causes, Effects, and Prevention
Fetal Alcohol Syndrome, often abbreviated as FAS, is a serious condition that affects children whose mothers consumed alcohol during pregnancy….
Factor V Leiden (Blood Clotting Disorder): Overview, Symptoms, Diagnosis & Management
Factor V Leiden, often abbreviated as FVL, is a genetic condition that affects the way blood clots. This disorder increases…
Fabry Disease: A Comprehensive Overview of Symptoms, Diagnosis, and Treatment
Fabry Disease (FD) is a rare genetic disorder that affects multiple systems in the body. It is caused by mutations…
Familial Mediterranean Fever (FMF): A Detailed Overview
Familial Mediterranean Fever, commonly abbreviated as FMF, is a rare genetic disorder that primarily affects people of Mediterranean descent. This…