Abstract
BACKGROUND: Hutchinson-Gilford Progeria Syndrome (HGPS) is a very rare genetic disorder with a frequency of 1 in 8 million live births. It is characterized by premature aging phenotype. The median age at death is 13.4 years
Recommended Citation
albahadle, Abdul-Karem Jasem
(2010)
"Progeria,"
Iraqi Postgraduate Medical Journal: Vol. 9:
Iss.
2, Article 20.
Available at:
https://www.ipmj.org/journal/vol9/iss2/20
COinS