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Molecular Diagnostics

What is Molecular Diagnostics?

Molecular Diagnostics involves the study of molecular and genetic markers within cells to detect abnormalities at the most fundamental level. Unlike conventional diagnostics, it focuses on understanding the genetic and molecular basis of diseases, enabling healthcare professionals to:

  • Detect diseases earlier and more accurately.
  • Identify specific pathogens and infections.
  • Tailor treatment plans based on a patient’s genetic makeup.

Applications of Molecular Diagnostics:

  • Infectious Diseases:
    • Rapid identification of viruses, bacteria, and fungi (e.g., COVID-19, HIV, Hepatitis).
  • Oncology:
    • Detecting cancer markers and mutations for personalized treatment strategies.
  • Genetic Testing:
    • Identifying hereditary conditions and assessing risks for genetic disorders.
  • Prenatal Screening:
    • Early detection of chromosomal abnormalities in fetuses.
  • Pharmacogenomics:
    • Analyzing how genes affect individual responses to medications.
  • Rare Diseases:
    • Uncovering the genetic causes of uncommon medical conditions.
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Benefits of Molecular Diagnostics:

  • High Sensitivity and Accuracy: Detects even minute changes in genetic material.
  • Personalized Medicine: Helps in tailoring treatments to individual needs.
  • Faster Results: Provides rapid and precise diagnostic insights.
  • Wide Disease Coverage: Applicable to infections, cancers, genetic disorders, and more.

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