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Werner syndrome: Werner syndrome is a premature aging disease that begins in adolescence or early adulthood and results in the appearance of old age by 30-40 years of age. (Source: Genes and Disease by the National Center for Biotechnology) ... more about Werner syndrome.
Werner syndrome: A form of premature aging where sufferers start aging during adolescence or soon after and appear old by the time they reach their 30's or 40's. Milder forms of the condition may also occur. More detailed information about the symptoms, causes, and treatments of Werner syndrome is available below.
See full list of 72 symptoms of Werner syndrome
Review possible medical complications related to Werner syndrome:
Research the causes of these diseases that are similar to, or related to, Werner syndrome:
See full list of 8 occasional symptoms of Werner syndrome
Medical news articles related to Werner syndrome include:
Source: HealthDay News
Medical research articles related to Werner syndrome include:
Click here to find more evidence-based articles on the TRIP Database
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Visit our research pages for current research about Werner syndrome treatments.
The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Werner syndrome include:
Read more about Clinical Trials for Werner syndrome
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Werner syndrome is a premature aging disease that begins in adolescence or early adulthood and results in the appearance of old age by 30-40 years of age. (Source: Genes and Disease by the National Center for Biotechnology)
Werner Syndrome (WS) is an inherited disease characterized by an early onset of atherosclerosis, osteoporosis, diabetes mellitus, and cancers of non-epithelial cell origin. Cultured cells from WS patients also present a shortened replicative lifespan and increased genetic instability. The genomic instability of WS cells is manifested at the cytogenetic level in the form of chromosome breaks and translocations, and at the molecular level predominately by multiple, large DNA deletions. (J. Biol. Chem., 273(51):34139-34144, 1998) - (Source - Diseases Database)
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