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"Progeria." Coping and Support. Mayo Foundation, 3 May 2014. Web. 16 Feb. 2016.

"Learning About
Progeria." Learning About Progeria. USA.Gov, 27 Dec. 2013. Web. 16 Feb. 2016.

"Progeria: Causes, Symptoms, and Treatments." WebMD. WebMD, n.d. Web. 17 Feb. 2016.

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Having a kid with progeria is hard because they will have a shortened live span on average they only live to about 14 years old. Also it will be very expenis=ve for you

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"Hutchinson-Gilford Progeria Syndrome." Genetics Home Reference. N.p., n.d. Web. 16 Feb. 2016.
"Progeria." - Mayo Clinic. N.p., n.d. Web. 16 Feb. 2016.
"About Progeria." Progeria Research Foundation. N.p., n.d. Web. 16 Feb. 2016.

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About 1 out of every 5 million new borns get progeria. It had been found in over 40 countries.

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http://2011gtms8e.wikispaces.com/file/view/Jia_L_punnet.JPG/230368604/640x480/Jia_L_punnet.JPG

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https://www.google.com/url?sa=i&rct=j&q=&esrc=s&source=images&cd=&cad=rja&uact=8&ved=0ahUKEwiuqM272fzKAhWimoMKHR5kCpwQjRwIBw&url=https%3A%2F%2Fwww.haikudeck.com%2Fprogeria-slide-science-and-technology-presentation-K3fihiV6H0&bvm=bv.114195076,d.amc&psig=AFQjCNF6N-9YncY4FJ_OdU4mk4Y3cP63Mg&ust=1455726173141216

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The LMNA produces a lamin A Protein which is the structure that holds the nucleus of a cell together. The abnormal lamin A protein that causes progeria is called progerin. Progerin makes the nucleus unstable. The gene that causes progeria is a Dominat gene.

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Lonafarnib was originally made to treat cancer but was found effective for progeria. It improves patients in many ways:
Gaining additional weight
Better hearing
improved bone structure
increased flexibility of blood vessels

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With progeria you get a higher risk of heart problems and strokes and that is the main cause of death. Usually a child lives to about 13 years old. Some kids die younger and some live to 20 and older.

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Hair loss (alopecia)
Aged-looking skin
Joint abnormalities
A loss of fat under the skin

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It is classified as single gene defect. It is autosomal dominant condition, and is X-linked dominant.

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Progeria is due to a "misspelling" in a gene on chromosome 1 that codes for lamin A. Misspelling in the lamin A gene is a substittion of just a single DNA base. Its a change from cytosine (C) to thymine (T).

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It is also called Hutchinson-Gilford progeria syndrome and benjamin button disease.