More than 6,000 genetic disorders cause children to deform and die

Common monogenic diseases in children today include: myelodystrophy with an incidence of 1/10,000, incomplete musculoskeletal muscle formation at the rate of 1/15,000 – 1/25,000, Dunchenne muscular dystrophy seen in 1/3,500 boys, root muscular dystrophy 20-40/1,000,000, congenital hemolysis A and B 10/10,000 boys…

Children with severe diseases need blood transfusions and iron discharge for life.

The majority of children with genetic disorders are born to perfectly healthy parents, with no history of the disease.

However, the healthy couple can still carry the mutated gene in the body (in the recessive form).

This group has a 25% risk of having children with monogenic disorders.

Experts said many families only know that the body has a mutated gene when giving birth to a sick baby.

There are people who become pregnant 4-5 times, all giving birth to babies with diseases, thereby completely losing faith in a healthy child.

“There are children who, born, have not seen anything, but a few years later naturally can’t walk anymore.

The child is completely awake, goes to school but does not develop as usual, the family is very difficult,” added experts.

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