Understanding Alkaptonuria: Causes and Effects

Alkaptonuria is a rare inherited metabolic disorder that affects the body's ability to break down certain compounds, specifically homogentisic acid. This condition arises due to a deficiency in the enzyme known as homogentisic dioxygenase (HGD). In a healthy individual, HGD plays a crucial role in the catabolism of tyrosine, an amino acid, converting homogentisic acid... Continue Reading →

Understanding Pheochromocytoma: Causes and Symptoms

Pheochromocytoma is a rare tumor that develops in the adrenal glands, typically originating from chromaffin cells, which are responsible for producing catecholamines such as adrenaline and noradrenaline. These hormones play a crucial role in the body's fight-or-flight response, regulating blood pressure and heart rate. When a pheochromocytoma occurs, it leads to excessive secretion of these... Continue Reading →

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