Progeria Syndrome

July 30, 2011 by admin · Leave a Comment · 345 views
Filed under: Diseases, Health Care and News 

progeria, progeria syndromeNew study could supply aid to children with a uncommon problem that triggers them to age at ten times the standard rate. But a new research inside the journal Science Translational Research in folks with progeria shows that this protein has an on-and-off change, providing scientists insight into how individuals, even without having the syndrome, age.

There is at present no set up remedy for progeria, however the study shows that an immune-suppressing drug called rapamycin could possibly be promising in clearing progerin from cells, thereby stopping the aging approach, Science reported.

What is Progeria?

According to MayoClinic, Progeria is a progressive genetic disorder that causes children to age rapidly, beginning in their first two years of life.

Children with progeria, also known as Hutchinson-Gilford progeria syndrome (HGPS), generally appear normal at birth. By 12 months, signs and symptoms, such as slow growth and hair loss, begin to appear.

Progeria Symptoms

Signs and symptoms of this progressive disorder include:

  • Slowed growth, with below-average height and weight
  • A narrowed face and beaked nose
  • Hair loss (alopecia), including eyelashes and eyebrows
  • Hardening and tightening of skin on trunk and extremities (scleroderma)
  • Head disproportionately large for face
  • Thin lips
  • Visible veins
  • Prominent eyes
  • Small lower jaw (micrognathia)
  • High-pitched voice
  • Delayed and abnormal tooth formation
  • Diminished body fat and muscle
  • Stiff joints
  • Hip dislocation
  • Insulin resistance
  • Irregular heartbeat

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