How is Progeria transmitted?

Answers:
Progeria has be determined to be genetic, that is, the disease is passed along during cell division contained by the formation of a fetus. However, it's not exactly hereditary because parents of children beside progeria are not affected, nor do they take a gene for it. The gene is on a normal chromosome (piece of genetic material) that have mutated during cell division (probably during formation of the gamete, i.e. egg or sperm cell). That mutation is then replicated during subsequent divisions. The produce for this mutation is unknown.
The gene for progeria is probably located on Chromosome 1 (of 46 pairs); other, similar diseases may be due to problems with different chromosomes. Studies done surrounded by the 1970’s show the mutation is autosomal dominant. This finding means that the mutation one and only has to come about on one of the chromosomes in a set of two, and the affected child will hold the condition. It also means that any children of an artificial person will own that condition.
For more info check the websites I've listed or Google investigate on "progeria genetics".

its a genetic conditon . to get it u must be born beside it .. but a very in danger of extinction one

If you go to Google and type surrounded by.

adult beginning progeria

.then you bring back to lots of links such as

http://www.bookrags.com/sciences/genetic.

that discuss both "Werner's syndrome (adult-onset progeria) and Hutchinson-Gilford syndrome (juvenile-onset progeria)"
as well as "various other less recognized forms of progeria" and "Inheritance of Progeria".

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How is Progeria transmitted?

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