2. HISTORY
It was also described independently in a academic
journal by Dr. Jonathan Hutchinson in 1886 and
Dr. Hastings Gilford in 1897.
The condition was later named Hutchinson-Gilford
progeria syndrome.
The word progeria comes from the Greek words
“pro” meaning “before” or “premature”, and
“geras” meaning “old age”.
3. WHAT IS PROGERIA?
Progeria is also known as Hutchinson-Gilford
Progeria Syndrome(HGPS)
It is a rare and very fatal genetic condition
Premature aging
6. SIGNS & SYMPTOMS
Limited growth
Loss of hair
early sings of skin aging, including thin skin
Visible veins
Loss of eyebrows and eyelashes
Loss of body fat
7. DIAGNOSIS PROCESSES
Plotting measurements on a normal growth curve
chart.
Testing hearing and vision.
Measuring vital sings, including blood pressure.
Looking for visible sings and symptoms that are
typical of progeria.
Measuring height and weight.
9. POTENTIAL FUTURE TREATMENT
Studying genes and the course of disease to understand
how it progresses. This may identify new treatments.
Studying way to prevent heart and blood vessel disease.
Performing human clinical trials using drugs known as
farnesyltransferase inhibitors (FTIs) such as lonafarnib.
10. PREVENTION
However, it has been recently discovered that FTIs, a
drug that has a possibility to help cure progeria,
might also be able to prevent the mishappen nuclei in
progeria cells.
12. CONCLUSION
Scientists are still looking for the to find the cure of this
abnormality syndrome.
Even though it has been seen for more than 100 years.
Progeria research foundation is now doing some DNA
mutation therapy to try to cure this disease.