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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
Keywords
Jasem albahadle, A. (2010). Progeria. Iraqi Postgraduate Medical Journal, 9(2), 221-224.
Abdul-Karem Jasem albahadle. "Progeria". Iraqi Postgraduate Medical Journal, 9, 2, 2010, 221-224.
Jasem albahadle, A. (2010). 'Progeria', Iraqi Postgraduate Medical Journal, 9(2), pp. 221-224.
Jasem albahadle, A. Progeria. Iraqi Postgraduate Medical Journal, 2010; 9(2): 221-224.
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