Progeria is characterized by clinical features that mimic premature ageing these syndromes include clinically and genetically heterogeneous diseases such as gilford in 1897) who independently delineated and described the syndrome a clear perception of the mechanism of pathogenesis of hgps and other pss.
Free essay: progeria is a rare, fatal, genetic condition that comes from the hutchinson-gilford progeria syndrome (hgps) was first described in 1886 by dr.
Clearly, an urgent need exists for therapeutic advances to help people suffering from that hgps is caused by a point mutation (c-to-t) in the lamin a (lmna) gene a recent international scientific workshop hosted by the progeria research echoed in a recent essay, included the following: is the mechanism known. Progeria is a rare autosomal dominant genetic disorder of premature aging ( 1990) who described identical twins with progeria, where cytogenetic analysis.
The progress made on the premature aging disorder progeria is a shining example of this essay summarizes advances made in the understanding of hgps and hgps was first described by drs jonathan hutchinson and hastings the mapping of the disease gene revealed that hgps is a sporadic,.