Newborn Screening Tests
Newborn Screening Tests To enable timely intervention and treatment, newborn screening tests are essential early diagnostic techniques
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Newborn Screening Tests To enable timely intervention and treatment, newborn screening tests are essential early diagnostic techniques
Genetic screening Test is a medical process used to assess an individual's genetic makeup for specific mutations, alterations, or
GeneXpert Test is a molecular diagnostic platform used to detect and identify specific pathogens, primarily bacteria or viruses, including. Mycobacterium
Urine Porphobilinogen (PBG) is a chemical compound involved in the biosynthesis of heme, a component of hemoglobin.
Tropheyma whipplei, Whipple's disease is a rare bacterial infection that primarily affects the gastrointestinal system. The condition
Wilson's Disease, Wilson's disease also known as hepatolenticular degeneration, is a rare genetic disorder that causes copper to accumulate
Blood Chromosome, Blood cells, specifically white blood cells, can be used to examine chromosomes. The human body's cells
Methaemoglobin (MetHb) is a form of hemoglobin that contains ferric iron (Fe3+) instead of ferrous iron (Fe2+), which is the
DNA Antibody, Anti-double stranded DNA (Anti-dsDNA) antibodies are a type of autoantibody produced by the immune system.
Acylcarnitines, Quantitative plasma acylcarnitine analysis is a laboratory test used to measure the levels of various acylcarnitine