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how many individuals get the progeria?

Progeria is a very rare genetic disease and can't be "caught." You are either born with it or not. If you are not born with it, you can never develop it.

The incidence of progeria is about 1 in every 8 million live births.

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14y ago

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What kind of disease is progeria?

Progeria is a disease of premature rapid aging. By the time individuals afflicted with progeria are just 5-7 years old, they can look like elderly people.


Can adults get Progeria?

No, adults can't get progeria, progeria is in the genes, so the person will be immediatly affected with it, you don't see adults with progeria, because most people with progeria die before they turn 13


Is progeria preventable?

Progeria is a genetic disease in which premature rapid aging occurs. Children at a relatively young age take on the appearance of old people, with wrinkles, joint pains, and the like. Progeria is not a communicable disease.


What limitations do people with progeria have?

People with progeria have limitations such as growth retardation, early aging symptoms (wrinkled skin, hair loss), cardiovascular problems, joint stiffness, and reduced bone density. These limitations can impact mobility, physical development, and overall quality of life for individuals with progeria.


Did Tom Cruise have progeria?

No, Tom Cruise has never had progeria.


How many people in America have progeria?

It is estimated that there are around 250-350 individuals living with progeria worldwide, with a small percentage of these individuals residing in the United States. The exact number of people in America with progeria may vary as new cases are diagnosed and reported.


Is progeria a dominant or recessive gene?

progeria is recessive, that's an easy question, dont be dumbactually progeria is dominant, according to the Progeria Research Foundation


Has anyone survives progeria?

The oldest person recorded with Progeria, was 21.


What is the progeria for karyotype?

Progeria, specifically Hutchinson-Gilford Progeria Syndrome (HGPS), is a rare genetic disorder caused by a mutation in the LMNA gene, which encodes the protein lamin A. This condition leads to accelerated aging in children, characterized by symptoms such as growth failure, hair loss, joint stiffness, and cardiovascular issues. The karyotype of individuals with progeria is typically normal, with no chromosomal abnormalities, but the mutation affects the structure and function of the lamin A protein, leading to the disease's symptoms.


Are there been any new genetic treatments to treat progeria?

There is no treatment for progeria. That is genetic aberration and not a disease.


What is premature old age called?

I believe it’s called Hutchinson-Gilford progeria syndrome


Are people with progeria obese?

The exact opposite. Children with Progeria are extremely skinny.