Thalassemia - Mylab | Translating Discovery to Delivery

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Thalassemia - Mylab | Translating Discovery to Delivery

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Thalassemia

A genetic disorder passed from parents to children, it’ a state where the body produces insufficient quantities of haemoglobin, an essential element of the red blood cells that help it get oxygen into the body. If detected in time, patients can be kept on regular blood transfusion for prolonged life.

* 0 /10000

Affects live births

* 0 %

Affects worldwide

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A genetic condition, it is best diagnosed by methodologies that drill down to molecular and genetic levels, MyLab’s forte.

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Molecular

ᵦ Thalaissemia Mutation Detection Kit

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Compact Q is Fluorescence Quantitative Polymerase Chain Reaction (PCR) Detection System.

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