Professor David Gems at the University of Missouri at Columbia has this viewpoint about distinctive again disorders:

“The potential value of understanding the causes of diseases such as Werner Syndrome is hard to overstate. Nowadays those involved in aging research increasingly view a

that is such a dramatic feature of this disease.

the mechanism that underlies all diseases of aging,

which appears in part to be cell slow down,

The first year or two of life, the scalp and hair is sparse. For a short amount of time, the hair stays the same as is at the time of birth. When the patient started to grow hair, the aging rapidly starts. The hair changes to either white or blonde. Progeria patients have no eyelashes or eyebrows and very few pubic and facial hairs (DeBusk 4).

Progeria patients do not suffer from mental diseases associated with aging (for example, Alzheimer). Progeria is not hereditary, therefore cannot be passed from generation to generation. Theorically speaking, every year is another decade for a child with Progeria. Socially, the child tends to be shy around strangers because they are aware of their appearance. When around friends and family they are friendly, witty, and mischievous. A child with the Progeria disease have average or above average intelligence. In general, Progeria patients have normal emotions; they are happy, sad, and angry in appropriate situations (DeBusk 6).

…studying Werner Syndrome could help pinpoint

Some topics in this essay:
Progeria Syndrome, Werner Syndrome, Similar Progeria, Aging Disorders, Syndrome Progeria, Progeria Socially, werner syndrome, Missouri Columbia, Alzheimer Progeria, Aging” November, Syndrome Schellenberg, aging process, fujiwara et al, fujiwara et, et al, progeria patients, aging disorders, child progeria, rapid aging, gems 1, child progeria disease, normal birth, werner syndrome progeria, progeria werner syndrome,