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 ……..
Alkaptonuria
Author: Dr. Arvind Kumar
Cleaning and Care of General Laboratory Glassware and Equipment
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 ……..
Phenylketonuria
Introduction Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency of the enzyme phenylalanine hydroxylase (PAH), which converts the amino acid phenylalanine to tyrosine. This leads to Read More ……..
Laboratory First aid (accidents)
Introduction Accidents in a medical or biochemical laboratory can occur at any time due to chemicals, glassware, heat sources, or electrical equipment. Every laboratory must be prepared with first aid Read More ……..
Laboratory Ethics
Introduction Medical Laboratory Ethics refers to the moral principles, standards, and practices that guide the behaviour and decision-making of professionals working in medical laboratories. These ethics ensure that laboratory activities Read More ……..