Sturge-Weber Syndrome: Causes, Symptoms & Diagnosis
Sturge-Weber Syndrome (SWS), or encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder caused by a mutation in the GNAQ gene. It leads to abnormal…
Sturge-Weber Syndrome (SWS), or encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder caused by a mutation in the GNAQ gene. It leads to abnormal…
Acute kidney failure (AKF), also known as acute renal failure, is a serious condition where the kidneys suddenly become unable to filter waste products from the…
Tularemia is a rare infectious disease that you may encounter in certain environments. It is caused by the bacterium known as Francisella tularensis, often called “rabbit…
Aortic coarctation is a congenital heart defect where a segment of the aorta is narrower than usual. This narrowing disrupts normal blood flow through the artery,…
E. coli (Escherichia coli) enteritis results from an infection by E. coli bacteria, causing inflammation and irritation in the intestines. This inflammation is the body’s response…
An itchy mole, typically a small, colored spot formed by clustered pigment cells (melanocytes), is a common skin growth. While moles may be present from birth,…
Low hCG levels indicate hCG concentrations below the expected range for a specific stage of pregnancy. This hormone is vital for early pregnancy support, and its…
Vernal conjunctivitis, also known as spring keratoconjunctivitis, is a chronic form of “pink eye” prevalent in warm climates. It typically begins in the spring and extends…
KD (KD), also known as mucocutaneous lymph node syndrome, is characterized by inflammation in the walls of blood vessels and lymph nodes. It affects blood flow…
Polio, also known as poliomyelitis, is a highly infectious disease caused by the poliovirus and primarily affects children under the age of five. While vaccinations strategies…