Find all needed information about Werner Syndrome Support. Below you can see links where you can find everything you want to know about Werner Syndrome Support.
http://www.het-werner-syndroom.com/english/index.html
This is a website for patients or relatives of patients who are interested in the very rare condition the Werner syndrome (WS). The reason for this website is because there is still no peer support group for the Werner Syndrome. For patients and their family there is now a possibility to connect and support …
http://www.wernersyndrome.org/registry/registry.html
Werner Syndrome was first described by Dr. Otto Werner at the Kiel University in 1904 (Werner, 1904). In his thesis, Dr. Werner described scleroderma-like skin and cataracts in a sibship. Because this disorder shares some aspects of aging as described for two Japanese-American sisters, WS has been described as the "caricature of aging" (Epstein et al., 1966).
https://ghr.nlm.nih.gov/condition/werner-syndrome
Oct 29, 2019 · Werner syndrome is inherited in an autosomal recessive pattern, which means both copies of the WRN gene in each cell have mutations. The parents of an individual with Werner syndrome each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.
https://www.dermatologyadvisor.com/home/decision-support-in-medicine/dermatology/werner-syndrome/
Werner syndrome (WS) is a type of progeroid syndrome characterized by the development of premature aging. ... No sponsor or advertiser has participated in, approved or paid for the content provided by Decision Support in Medicine LLC. The Licensed Content is the property of and copyrighted by DSM. Powered By Decision Support in Medicine. Jump ...Author: Randy Tang
https://en.wikipedia.org/wiki/Werner_syndrome
Werner syndrome (WS) (sometimes Werner's syndrome), also known as "adult progeria", is a rare, autosomal recessive disorder which is characterized by the appearance of premature aging.. Werner syndrome is named after the German scientist Otto Werner. He identified the syndrome in four siblings observed with premature aging, which he explored as the subject of his dissertation of 1904.Specialty: Endocrinology
https://rarediseases.info.nih.gov/diseases/7885/werner-syndrome
66 rows · Feb 21, 2019 · Werner syndrome is a condition that causes premature aging. People with …
https://www.ncbi.nlm.nih.gov/books/NBK1514/
Dec 02, 2002 · Werner syndrome is characterized by the premature appearance of features associated with normal aging and cancer predisposition. Individuals with Werner syndrome develop normally until the end of the first decade. The first sign is the lack of a growth spurt during the early teen years. Early findings (usually observed in the 20s) include loss and graying of hair, hoarseness, and scleroderma ...
https://www.diseaseinfosearch.org/disease/7471
Werner syndrome is a rare genetic condition that causes accelerated aging. Affected individuals usually display normal growth and development during childhood but then lack a normal growth spurt at puberty. As a result, they are typically short in height.
https://www.ncbi.nlm.nih.gov/books/NBK22252/
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. Its physical characteristics may include short stature (common from childhood on) and other features usually developing during adulthood: wrinkled skin, baldness, cataracts, muscular atrophy and a tendency to diabetes mellitus, among others.
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