HeMe #4 | Page 14

PROGERIA–One of the rarest Progeria, also known as Hutchinson-Gilford progeria syndrome is a very rare genetic disease. Progeria is characterized by "before" or "premature" aging. This disease influences the skin, musculoskeletal system, and vasculature. According to greek nomenclature progeria means the early old age. Progeria will lead to premature death due to atherosclerosis in the coronary vessels and carotid arteries. The babies usually look normal at birth, but when they grow up signs start to appear. Classic onset of this disease is before the 3rd year of life mostly in 6 to 12 months. Initially the patients with this disease show changes in their skins . Skin becomes rough and without hair (alopecia). Restricted weight gain and physical growth. Face looks old to the age with prominent eyes and beaked nose.