Progeria Hutchinson-Gilford Disease: General Information

Hutchinson-Gilford Progeria Syndrome is the most common type of progeria disease. There are other progeria syndromes such as Progeria Werner and Progeria Wiedemann-Rautenstrauch. But what will be discussed here is Hutchinson-Gilford Progeria Syndrome.

This type of progeria can make the baby's physically aging too quickly. This rapid aging process will begin in the first two years after birth. Progeria disease is not contagious and not a hereditary disease, it can happen to anyone regardless of gender or race.

Worldwidely, there is only one in four million babies are born with this condition. Infants with progeria generally have only a life expectancy of up to 13 years, but some survive for up to 20 years or more.

Progeria Hutchinson-Gilford Disease
Progeria Hutchinson-Gilford Disease: General Information

Progeria Hutchinson-Gilford Disease Symptoms


Infants with progeria generally appear normal at birth. Progeria begins to show its symptoms in the first few months after birth. Initially, infants with progeria will show symptoms of slowing growth process, can be seen from the weight of infants who are difficult to increase.

Some people with progeria have skin that looks like scleroderma in the arms and legs. However, the development of motor and intelligence of infants with progeria still runs like in general.

Generally, infants with progeria have small physical and weak, such as physical elderly. Some physical conditions as well as infant health that can be a symptom of progeria are:
  • His voice is loud and high pitched.
  • Skin wrinkles, spots appear, and thinning.
  • Gear growth becomes slow and not normal.
  • Hair loss, including eyelashes and eyebrows.
  • Blood vessels under the skin can be seen clearly.
  • Leaf ear widened.
  • A large eyeball protrudes outward, and the eyelids can not be perfectly closed.
  • Body fat and muscle slowly disappear.
  • The size of the head is not proportional, looks big compared to his body.
  • The size of the face narrowed (petite) and lower jaw smaller.
  • Hearing deteriorates.
  • Brittle bones.
  • Dislocation of the pelvis.
  • Heart disease and blood vessels are quite severe.
  • Resistance to insulin.
  • Rigid joints.
  • The connective tissue and skin harden and thicken resembles scleroderma.

Diseases that generally affects people aged 50 years and over will usually be experienced by infants with progeria as he grew. Even heart attacks or strokes become one of the biggest causes of death of progeria sufferers.

It is advisable to consult your doctor immediately if your baby or child grows and develops abnormally.

Thats all the general information about Progeria Hutchinson-Gilford Disease. Even though this particular progeria disease is rare to be found, this disease is a deadly one.

Progeria Hutchinson-Gilford Disease: General Information