This diagnostic process is a speedy screening methodology employed to detect the presence of irregular hemoglobin, particularly hemoglobin S (HbS), the variant related to a selected blood dysfunction. It depends on the precept that HbS, when deoxygenated, types polymers that cut back the answer’s readability, inflicting turbidity. A constructive consequence signifies the potential presence of the situation, prompting additional confirmatory testing.
The examination provides a comparatively cheap and available technique of preliminary evaluation, significantly precious in resource-limited settings or for large-scale screening packages. Traditionally, this methodology performed a vital function in figuring out people carrying the trait, permitting for knowledgeable genetic counseling and preventative measures. Its simplicity permits for fast outcomes, facilitating well timed intervention.
