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what causes the disorder

The mutations is in both sexes and is inhearited from the parents.This affects about 33% of prople in the world.

the different names

one name it has is muscular dystrophey the sickness affects the bodys musclar growth. This is the only other name

what gene or chromosomes is affected

The X chromosomes are the most infected but only by males. Females can have some severe cases but its not usual

Are there prenatal tests

Yes the tissues from the placenta can be analyzed to see if they are infected after birth.

What are the symptoms

enlarged calf muscles, being clumsy, falling often, trouble running and walking, difficulty getting up

what population is affected

1 out of 38,000 people around the world are affected and they have to be a boy under the age of 13 but the chance is still slim

how is it inherited

Mostly men but its a recessive gene it is vary rare for a female to have it.

what kind of medical assistance will the affected child need

they will need a wheelchair help walking and a standing platform

Duchenne syndrome

Are there treatments or cures

There is no cure but treatment can make there life better it can let them be mobile and more independent

what is the current status of resarch on this disorder

The treatment is affordable and is offered to everyone everywhere

could this disorder have been prevented?

not really it happenes to the male most of the time and is passed down form generation to generation

can individuals have children in the future

yes but they will have a 50% chance of getting the sickness

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