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Progeria information
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Information on Progeria

 
 
      Progeria is an autosomal dominant genetic disorder cause by a random mutation of a chromosome. The cause of this mutation is unknown. The name progeria comes from a Greek word meaning "prematurely old".
     

      There are 2 main progeroid sundromes, Werner's Syndrome and Hutchinson-Gilford Syndrome. Werner's Syndrome begins at the onset of puberty, whereas Hutchinson-Gilford is evident in the 1st yeas of life. Another notable difference is the presence of cancer as a symptom in Werner's Syndrome. The symptom of cancer is acsent in Hutchinson-Gilford Syndrome.

 

      Huchinson-Gilford Syndrome was 1st described in 1886. It is known as the "progeria of childhood." Werner Syndrome is commonly known as "progeria of the adult" and was 1st described in 1904.

 

      Both of these conditions are chatacterized by rapid aging. Affected persons experiance all the changes of the aging process at about 7 times the rate of a normal person. Since there is no specific tests for progeria, diagnosis is made based on symptoms.

 

      Hutchinson-Gilford Syndrome begins in the first years of life years of life with an average life span of 12 years. Since it's discorvery, 100 cases have been reported.Werner's Syndrome begins at puberty and the average life span is 20-30 years.

 

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