Hypercholesterolemia: Causes, Symptoms, and Treatment
Hypercholesterolemia refers to abnormally high levels of cholesterol in the blood. Cholesterol is a waxy substance essential for cell formation, but excessive amounts can increase…
Hypercalcemia Treatment Adjunct: Comprehensive Guide
Hypercalcemia is a medical condition characterized by elevated calcium levels in the blood. While mild cases may be asymptomatic, severe hypercalcemia can lead to critical…
Hypercalcemia Due to Primary Hyperparathyroidism
Hypercalcemia, a condition characterized by elevated calcium levels in the blood, is commonly associated with primary hyperparathyroidism (PHPT). This endocrine disorder occurs due to excessive…
Hypercalcemia Associated with Sarcoidosis
Hypercalcemia associated with sarcoidosis is a medical condition characterized by elevated calcium levels in the blood due to the granulomatous inflammation seen in sarcoidosis. Understanding…
Hypercalcemia: Causes, Symptoms
Hypercalcemia refers to an elevated calcium level in the blood above the normal range. Calcium is vital for bone health, muscle function, nerve transmission, and…
Hyperbilirubinemia Due to Hemolytic Disease of the Newborn
Hyperbilirubinemia in newborns caused by hemolytic disease is a serious condition that requires prompt diagnosis and management. Hemolytic disease of the newborn (HDN) is characterized…
Hyperbilirubinemia: Causes, Symptoms, and Treatment
Hyperbilirubinemia is a medical condition characterized by elevated levels of bilirubin in the blood. Bilirubin is a yellow pigment formed during the breakdown of red…
Hyperammonemia Due to Propionic Acidemia
Hyperammonemia due to propionic acidemia (PA) is a severe metabolic condition resulting from the accumulation of ammonia in the bloodstream. Propionic acidemia is a rare…
Hyperammonemia Due to Methylmalonic Acidemia
Hyperammonemia due to methylmalonic acidemia (MMA) is a rare yet serious metabolic disorder characterized by elevated ammonia levels in the blood. This condition arises from…
Hyperammonemia Associated with N-Acetylglutamate
N-Acetylglutamate Synthase (NAGS) deficiency is a rare autosomal recessive metabolic disorder that disrupts the urea cycle. This condition results in the accumulation of ammonia in…