G6PD deficiency disease Genetics from parents to children

A genetic disease caused by a deficiency of the enzyme G6PD (glucose-6-phosphate dehydrogenase), which is an important enzyme in various cells. throughout the body, especially red blood cells Its function is to help protect cells. from the destruction of free radicals People with this enzyme deficiency have red blood cells that break easily when exposed to various stimuli, such as certain foods, certain drugs, and infections, causing various symptoms.

Causes of G6PD deficiency

This disease is a type of hereditary disease. The recessive genes on the X chromosome (X-linked recessive) are passed on from mother to baby. This gives sons a 50 percent chance of having G6PD deficiency, and daughters a 50 percent chance of being carriers of the disease.

Symptoms of G6PD deficiency

When people with this condition are stimulated, the hemolysis of red blood cells occurs. There will be various symptoms as follows:

Factors that trigger hemolysis

How should people with this condition behave?