Hutchinson-Gilford Progeria Syndrome is a very rare disease that is caused by several different mutations in the lamin A gene.If you were to culture cells from patients who have Progeria,what effect might you expect to see over time?

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Hutchinson-Gilford Progeria Syndrome is a genetic disorder that affects the structure of the nuclear envelope, causing it to become irregularly shaped. This can result in a variety of cellular abnormalities, including altered gene expression, impaired signaling pathways, and changes in cellular architecture. Over time, these effects can lead to a variety of symptoms, including premature aging, brittle bones, cardiovascular disease, and other health problems.

Hutchinson-Gilford Progeria Syndrome Is a Very Rare Disease That Is