Von Willebrand Disease: Types, Causes & Symptoms
Von Willebrand Disease (VWD) is a genetic disorder that affects the ability of blood to clot properly due to a deficiency in the von Willebrand factor…
Von Willebrand Disease (VWD) is a genetic disorder that affects the ability of blood to clot properly due to a deficiency in the von Willebrand factor…
Apert syndrome is a rare genetic disorder classified under the category of skull development syndromes. It is characterized by the premature fusion of the coronal sutures,…
A branchial cleft cyst may form on either side of the neck or just beneath the collarbone. This condition is linked to anomalies when the structures…
Aicardi syndrome is a rare neurological and genetic disorder that primarily affects females. It is characterized by the partial or complete absence of the corpus callosum,…
Preeclampsia is a complication estimated to be present in around 5-7% of all pregnancies and is one of the leading causes of maternal morbidity worldwide. This…
Bleeding esophageal varices are a medical emergency characterized by the rupture and bleeding of blood vessels in the esophagus. This condition is typically associated with severe…
Alkaptonuria, also known as black urine disease, is a rare genetic disorder that affects the body’s ability to break down the amino acids tyrosine and phenylalanine….
Anaphylaxis is a severe allergic reaction with a rapid onset that escalates into a life-threatening emergency upon exposure to specific allergens. While these allergens are typically…
Chickenpox, also known as varicella, was common until the 1995 vaccine was introduced. Itchy rashes with small, fluid-filled blisters characterize this highly contagious illness. Effective immunization…
Erythrocytosis is characterized by an unusually high number of red blood cells (RBCs) or erythrocytes in the bloodstream, increasing blood viscosity. This elevated cell count can…