MOLECULAR DETECTION OF INHERITED HAEMATOLOGICAL DISORDER

Abstract

A human disease studies on molecular level and its diagnostics are result of our approach towards our aim to look after patients in their absolute genetic needs from counseling to DNA profiling for disease prevention, by performing entire genetic tests from hereditary diseases to infectious diseases from introduction of individualized medicines to prenatal diagnosis from non-invasive methods. Molecular Diagnosis of disease is very useful way to detect abnormalities in DNA level. These techniques are rapid, pragmatic advancement making them cost effective, accurate and setting gold standards. Various diseases i.e. Infectious (Viral, Bacterial, Fungal), Inherited and Malignancies can be detected in early stages to start medication and treatment that will reduce convalescence, monetary loss, mental stress and untimely demise. These molecular approaches should be made as an integral part of medical investigation to detect early to treat early approach in betterment of all over Health status of population at large.