… Almost all individuals with HGPS have the disorder as the result of a de novo autosomal
dominant pathogenic … HGPS is also referred to as the Hutchinson-Gilford syndrome or progeria. …

… Hutchinson–Gilford progeria syndrome (HGPS) is a rare but well known entity characterized
by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, …

… and Lmna L530P knockin will help the study of progeria. Lmna mutations have also recently
been found in patients with atypical forms of progeria. The discovery of the HGPS mutations …

… as the Hutchinson–Gilford syndrome, progeria, or progeria of … premature aging, progeria
patients do not appear to have … from the expression of the progeria mutation. Based on limited …

… advances in understanding this syndrome may offer insight … accelerated in the
Hutchinson–Gilford progeria syndrome, an … characteristics of Hutchinson–Gilford progeria …

… Estos médicos describieron la progeria por primera vez, por lo que en la literatura … (Hutchinson-Gilford
progeria syndrome) (HGPS, MIM–17667), también denominada progeria infantil. …

Aging, the main risk factor for cardiovascular disease (CVD), is becoming progressively more
prevalent in our societies. A better understanding of how aging promotes CVD is therefore …

… Progeria is sporadic, very rare, autosomal dominant, deadly childhood disorder. It is one of
the progeroid syndromes also known as Hutchinson–Gilford progeria syndrome … progeria and …

… Hutchinson-Gilford progeria syndrome (HGPS) is a rare human genetic disease that leads
to a severe premature ageing phenotype, caused by mutations in the LMNA gene. The LMNA …

… and mechanisms of this syndrome as a … Hutchinson-Gilford progeria syndrome and the
need for more studies on the pharmacologic and pharmacogenomic approach to this syndrome…