Alkaptonuria: Causes, Symptoms & Diagnosis
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….
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…
Hemophilia is a rare condition that affects the body’s ability to clot blood, leading to excessive bleeding even from minor injuries. Although it is usually inherited,…
Acromegaly is a rare hormonal disorder where the anterior pituitary gland produces too much growth hormone (GH), mostly affecting adults aged 30 to 50. This excess…
Wilson’s disease is a rare genetic disorder that disrupts copper metabolism in the body. This condition is also referred to as progressive lenticular degeneration or hepatolenticular…
Hyperopia, often referred to as farsightedness, is a vision condition characterized by clearer vision of distant objects compared to nearby ones. This occurs due to how…
Endometriosis is a reproductive condition often diagnosed in women aged 25 to 40, though it can develop as soon as menstruation begins. It involves tissue similar…
A bezoar is a mass trapped in the digestive tract, such as the stomach, small intestine, or colon. It can be composed of different materials, such…