Wilson’s Disease: Risk Factors, Causes & Symptoms
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…
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…
Krabbe disease, or globoid cell leukodystrophy, is a rare genetic disorder that impairs the nervous system. It stems from an enzyme deficiency needed to metabolize specific…
Nephroptosis, also known as a floating or wandering kidney, is a rare condition in which one or both kidneys shift into an incorrect location, particularly when…
A ventral hernia is a medical condition where an opening or weakness in your abdominal muscles allows tissues or organs, typically part of your intestines, to…
Cacosmia is a condition that affects your sense of smell and its pathways, leading you to perceive unpleasant odors that aren’t present in your environment or…
A corneal ulcer is an open sore that develops on the cornea, which is the clear, protective outer layer of your eye. If this condition is…
Russell-Silver Syndrome (RSS), also known as Silver-Russell Dwarfism or Silver-Russell Syndrome, is a rare genetic primordial dwarfism disorder primarily characterized by growth abnormalities, particularly growth restriction…