IMD Panel Test (IMD Panel Quantitative Blood Test)

What is the IMD panel test?

A significant class of metabolic-related genetic illnesses are called IMDs (inborn metabolic disorders). Enzymatic anomalies bring on these illnesses; because the enzyme cannot act on the substrate, toxic substances accumulate in the body and disrupt healthy biological processes. When these anomalies are discovered by newborn screening in the asymptomatic stage, time management can begin. The IMD panel test investigates the amino acid (the protein's building block), organic acid, and fatty acid oxidation abnormalities for inborn metabolic diseases (IMD).

When is the IMD panel quantitative blood test done?

A doctor may recommend this test when he suspects

• Lethargy symptoms that alter over time
• Critically ill newborn with a history of getting worse following an illness that happened during a straightforward pregnancy
• Nervous system symptoms brought on by concurrent illnesses or stress

What are the components of the IMD panel test?

The components include detecting organic acids, amino acids, and fatty acids. IMD test can detect specific inborn errors of metabolism. Some of these disorders cannot be detected early.

How is the IMD panel test done?

• A blood sample is collected from the vein of the adults or by a heelprick in the newborns.
• All the clinical details and drug history must accompany the sample.
• The report usually comes after 3 Days