Progeria is a very rare disease that affects about one in 18 million children and results in premature aging and death in adolescence from complications of cardiovascular disease. In a study on mice and human cells, researchers ...
Nov 18, 2019
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Progeria, which develops from a rare genetic mutation, causes the same symptoms in children as in 80-year old people: brittle bones, longer healing times, and heart disease, among others. Affecting randomly about one in every ...
Aug 23, 2019
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Researchers at the Centro Nacional de Investigaciones Cardiovasculares (CNIC) and the Universidad de Oviedo have discovered a new molecular mechanism involved in the premature development of atherosclerosis in mice with Hutchinson-Gilford ...
Mar 12, 2019
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Aging is a leading risk factor for a number of debilitating conditions, including heart disease, cancer and Alzheimer's disease, to name a few. This makes the need for anti-aging therapies all the more urgent. Now, Salk Institute ...
Feb 19, 2019
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Spinal muscular atrophy (SMA) is a genetic disease that can leave infants with weak muscles and trouble breathing. Many with the disease die before age two. To help these patients, doctors need therapies that target the genetic ...
May 8, 2018
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A report from a clinical trial for a drug to treat the rapid-aging disorder progeria, published in this week's Journal of the American Medical Association, offers hope for families with the ultra-rare genetic condition.
Apr 27, 2018
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Scientists from the University of Cambridge have identified a potential therapeutic target in the devastating genetic disease Hutchinson-Gilford Progeria Syndrome (HGPS), which is characterised by premature ageing.
Apr 27, 2018
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Children with a rare, incurable disease that causes rapid aging and early death may live longer if treated with an experimental drug first developed for cancer patients, a study suggests.
Apr 24, 2018
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In a recent paper published in Cell Reports, Saint Louis University researchers have uncovered new answers about why cells rapidly age in children with a rare and fatal disease. The data points to cellular replication stress ...
Mar 19, 2018
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Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare fatal genetic disorder which causes sufferers to age prematurely. In a new study in the journal Pediatric Research, which is published by Springer Nature, scientists ...
Jan 18, 2018
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