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Hip Disease in Hutchinson-Gilford Progeria Syndrome

Journal of Pediatric Orthopaedics, 1984
Two cases of Hutchinson-Gilford progeria syndrome are presented with a focus on hip disease. A severe coxa valga is the first abnormality. The femoral head becomes increasingly uncovered as the acetabulum becomes more dysplastic. The center edge angle decreases, the acetabular index increases, and the medial wall of the acetabulum widens.
openaire   +2 more sources

Vascular dysfunction in Hutchinson–Gilford progeria syndrome

Trends in Molecular Medicine
Most patients with Hutchinson-Gilford progeria syndrome (HGPS) succumb to cardiovascular disease. Recent studies by Barettino et al., Cardoso et al., and Vakili et al. utilized progeria mouse models to elucidate novel mechanisms by which vascular smooth muscle cell (VSMC) and endothelial cell (EC) dysfunction accelerate the progress of the disease ...
Yaping Zhao, Li Wang, Suowen Xu
openaire   +2 more sources

PROGERIA

American Journal of Roentgenology, 1968
F R, Margolin, H L, Steinbach
openaire   +2 more sources

Rhinoplasty on Hutchinson–Gilford Progeria Syndrome Patient

Aesthetic Plastic Surgery, 2021
Mauro Barone   +3 more
openaire   +2 more sources

Cardiovascular Progerin Suppression and Lamin A Restoration Rescue Hutchinson-Gilford Progeria Syndrome

Circulation, 2021
Sussan Nourshargh   +2 more
exaly  

DNA methylation signatures in Blood DNA of Hutchinson–Gilford Progeria syndrome

Aging Cell, 2022
Junko Oshima, Tanvir Alam, Thomas Haaf
exaly  

Hutchinson Gilford Progeria Syndrome

2009
Dieter Metze   +199 more
openaire   +1 more source

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