Introduction Lesch–Nyhan Syndrome (LNS) is a rare inherited metabolic disorder that primarily affects males and is caused by a defect in purine metabolism. It results from a deficiency of the Read More ……..
Simplifying Allied Health Learning.
Introduction Lesch–Nyhan Syndrome (LNS) is a rare inherited metabolic disorder that primarily affects males and is caused by a defect in purine metabolism. It results from a deficiency of the Read More ……..
Introduction Homocystinuria is an inborn error of metabolism characterized by excessive accumulation of homocysteine and its metabolites in blood and urine. It is primarily caused by defects in the methionine Read More ……..
Introduction Cell biology is often called the basic unit of life. Every living organism, from the simplest bacteria to the most complex human being, is built from cells. In the Read More ……..
Introduction Alkaptonuria is a rare inherited metabolic disorder characterized by the deficiency of the enzyme homogentisate 1,2-dioxygenase (HGD), leading to the accumulation of homogentisic acid (HGA) in the body. This Read More ……..
Introduction In any biochemical or medical laboratory, the accuracy and reliability of analytical results are directly dependent on the cleanliness of glassware and instruments. Even trace contamination—such as residual detergent, Read More ……..