Progeria Syndrome
New study could offer help to children having a rare issue that triggers them to age at ten times the normal rate. But a fresh research within the journal Science Translational Research in individuals with progeria shows that this protein has an on-and-off switch, providing scientists insight into how individuals, even without having the syndrome, age.
There exists presently no founded remedy for progeria, but the study reveals that an immune-suppressing drug called rapamycin might 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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