Progeria Report

Genetics determines the characteristics that individuals inherit from their parents. In today's society, the role of genetics is very important and they determine the physical appearance and personality. However, when a child is mutated in a gene, it may be transformed. A rare and fatal defect caused by this gene mutation is early aging. This disease is an unfortunate illness that can occur in two forms including Hutchison-Gilford Progeria or Werner's syndrome.

Premature aging is a very rare autosomal dominant disease and symptoms similar to aging appear at very young ages. Premature aging is one of several prostate syndromes. People born with premature aging usually live in their teens to early twenties. It is a genetic condition that occurs as a new mutation, and carriers are rarely inherited because they are not usually. The term premature aging applies strictly to all diseases characterized by premature aging symptoms and is often used in such diseases, but it is generally applied in particular to Hutchinson-Gilford early stage syndrome (HGPS) .

Otto Werner originally defined Werner's syndrome (WS) in 1904 based on scleroderma, thin, supple skin, and bilateral cataract. Williams syndrome is also known as progeria, premature aging and danger of adulthood. WS is the most common premature aging. Premature aging may also refer to Hutchinson - Guilford syndrome, which has been explained as a defect in the Lamin A gene and has been afflicted early in life. Premature aging comes from Greek and means "before gerontology". Please look at the picture below. The aging process involves errors in the mitotic machinery that divide the cells in the latter stages of life and hence WS serves as a model for studying the aging process in vivo and in vitro. However, many Williams syndrome patients experience early changes with age. Mental retardation was not observed