New Research Progeria Presented progeria indonesia

New Research Progeria– While New Research Progeria in translational science research journal in individuals with progeria shows that this protein has a switch on and off, giving an overview of how people learn, whether or not this syndrome age. There is currently no cure for progeria established, however, New Research Progeria found that a drug immunosuppression called rapamycin could be promising progerin compensation from the cells, thereby halting the aging method, Science reported.

New Research Progeria or Hutchinson-Gilford syndrome

New Research Progeria Progeria (also known as “progeria syndrome Hutchinson-Gilford”, “Hutchinson-Gilford syndrome,” and “progeria syndrome”) is an extremely rare genetic disease symptoms similar to those aspects of aging are manifested at an age early. Progeria word comes from the Greek word “pro” (πρό) means “before” and “Geras” (γῆρας) means “old.”


New Research Progeria said Disorder affects very low and occurs in about 1 in 8 million live births. Those who are born with progeria typically live in their teens and twenties. It is a genetic disease that appears as a new mutation (de novo), and is not inherited. Although progeria term applies strictly to all the diseases that are characterized by symptoms of premature aging, and is often used as such, is often applied specifically refers to Hutchinson-Gilford progeria.
Scientists are particularly interested in progeria because it might reveal clues about the normal aging process. Progeria was first described in 1886 by Jonathan Hutchinson.It was also described independently in 1897 by Hastings Gilford. The condition was later named Hutchinson-Gilford progeria in syndrome (HGPS).
Early symptoms include stunted growth and a skin condition similar localized scleroderma. As a child past infancy, additional conditions are visible. Limited growth, alopecia and a characteristic appearance (small face and jaw tip,) are New Research Progeria characteristic of progeria. People diagnosed with this disorder usually have fragile little bodies such as the elderly. Later condition causes wrinkled skin problems, atherosclerosis, kidney failure, vision loss, hair loss and cardiovascular disease. It is not transmitted by descent.
A child with this condition show signs of symptoms is usually around 18-24 months. After birth a healthy baby in the research, its size and weight suddenly, below the average for their age. People generally maintain normal mental and motor development. There are many signs and symptoms of this progressive disease, and tend to worsen as the child grows. The appearance of the face is often wrinkled, with a larger head relative to its body, with a narrow face and beak nose.


New Research Progeria The child experiences the whole body alopecia. Scleroderma, a hardening and narrowing of the skin on the trunk and limbs of the body, is also widespread. As experience hair loss, scalp veins are visible and prominent bulging eyes. Musculoskeletal degeneration causes loss of body fat and muscle, joint stiffness, hip dislocations, and other symptoms usually absent in non-elderly population.

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