Published November 6, 2018 | Version v1
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A BRIEF REVIEW ON HUTCHINSON-GILFORD PROGERIA SYNDROME

Description

Hutchinson-Gilford Progeria Syndrome (HGPS) was first documented in 1886 in the medical literature. A HGPS patient has the physical characteristics and appearances of an elderly individual. It is now clear that the syndrome results from the accumulation of a metabolite formed during processing of the mutated pre-lamin A protein. The purpose of this review is to increase the awareness of Hutchinson-Gilford Progeria Syndrome and its conditions and discuss the new therapeutic approaches among worldwide.

Key words: Hutchinson-Gilford Progeria Syndrome, bone deformation, pre-lamin A, Progeroid syndromes.

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