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I need to know for school

Thanks for the help (:

2007-10-25 09:24:53 · 2 answers · asked by Anonymous in Health Diseases & Conditions Other - Diseases

2 answers

Progeria

2007-10-25 09:31:23 · answer #1 · answered by greydoc6 7 · 2 0

The 'GreyDoc' has the correct answer. Read more from the Link below.

Progeria, also known as Hutchison-Gilford progeria syndrome (HGPS). In 2003, researchers announced the discovery of a single gene mutation responsible for Hutchison-Gilford progeria syndrome. The gene is known as lamin A (LMNA), which makes a protein necessary to holding the center (nucleus) of a cell together. Researchers believe the genetic mutation renders cells unstable, which appears to lead to progeria's characteristic aging process.

Unlike many genetic mutations, Hutchison-Gilford progeria isn't passed down in families. Rather, the gene change is a chance occurrence that researchers believe affects a single sperm or egg just before conception. Neither parent is a carrier, so the mutations in the children's genes are new (de novo).

There are, however, other progeroid syndromes that run in families. They include Wiedemann-Rautenstrauch syndrome and Werner's syndrome. In Wiedemann-Rautenstrauch syndrome, also known as neonatal progeroid syndrome, onset of aging begins in the womb, and signs and symptoms are apparent at birth. Werner syndrome begins in adolescence or early adulthood. These inherited progeroid syndromes also cause rapid aging and shortened life span.

Good luck.
DS

2007-10-25 09:52:56 · answer #2 · answered by Duck Soup 4 · 1 0

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