Werner syndrome: Difference between revisions

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==Overview==
==Overview==
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[[Werner's syndrome]] more closely resembles [[Accelerated aging disease|accelerated aging]] than any other segmental [[progeria]]. For this reason, Werner syndrome is often referred to as a progeroid syndrome, as it partly mimics the symptoms of [[Progeria]].
[[Werner's syndrome]] more closely resembles [[Accelerated aging disease|accelerated aging]] than any other segmental [[progeria]]. For this reason, Werner syndrome is often referred to as a progeroid syndrome, as it partly mimics the symptoms of [[Progeria]].


==History==
==History==
Werner's syndrome is named after [[Otto Werner]],<ref>{{WhoNamedIt|synd|892}}</ref> a German scientist, who, as a student, described the syndrome as part of his doctoral thesis in 1904.  
Werner's syndrome is named after [[Otto Werner]],<ref>{{WhoNamedIt|synd|892}}</ref> a German scientist, who, as a student, described the syndrome as part of his doctoral thesis in 1904.  


==Pathophysiology==
==Pathophysiology==
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[[Image:autorecessive.svg|thumb|left|Werner syndrome has an autosomal recessive pattern of [[Heredity|inheritance]].]]
[[Image:autorecessive.svg|thumb|left|Werner syndrome has an autosomal recessive pattern of [[Heredity|inheritance]].]]
==Natural history, Complications and Prognosis==
* Although the symptoms manifest after 10 years, the earliest person diagnosed was six years old.<ref name="Leis">Leistritz, F. NCBI. Werner Syndrome. Retrieved Jun 2, 2011, from http://www.ncbi.nlm.nih.gov/books/NBK1514/</ref> Following puberty, they age rapidly, so that by age 40, they often appear several decades older.
* In people with Werner syndrome, death usually occurs by [[myocardial infarction]] or [[cancer]]<ref name="Leis" />

Revision as of 14:55, 24 July 2012

Werner syndrome
ICD-9 259.8
OMIM 277700
DiseasesDB 14096
MeSH C16.320.925

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]

Overview

Werner Syndrome (WRN) is a very rare, autosomal recessive[1] disorder characterized by the appearance of premature aging.[2]

Werner's syndrome more closely resembles accelerated aging than any other segmental progeria. For this reason, Werner syndrome is often referred to as a progeroid syndrome, as it partly mimics the symptoms of Progeria.

History

Werner's syndrome is named after Otto Werner,[3] a German scientist, who, as a student, described the syndrome as part of his doctoral thesis in 1904.


Pathophysiology

Werner syndrome is an autosomal recessive disorder.[1] The gene associated with Werner Syndrome lies onchromosome 8 in humans.[4]The defect is on a gene that codes DNA helicase and it is located on the short arm of the 8th chromosome. The disorder is directly caused by shorter-than-normal length telomere maintenance. As a result DNA replication is impaired.

File:Autorecessive.svg



Natural history, Complications and Prognosis

  • Although the symptoms manifest after 10 years, the earliest person diagnosed was six years old.[5] Following puberty, they age rapidly, so that by age 40, they often appear several decades older.
  • In people with Werner syndrome, death usually occurs by myocardial infarction or cancer[5]
  1. 1.0 1.1 Ozgenc A, Loeb LA (2005). "Current advances in unraveling the function of the Werner syndrome protein". Mutation research. 577 (1–2): 237–51. doi:10.1016/j.mrfmmm.2005.03.020. PMID 15946710. Unknown parameter |month= ignored (help)
  2. Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA (1997). "The Werner syndrome protein is a DNA helicase". Nature genetics. 17 (1): 100�"3. doi:10.1038/ng0997-100. PMID 9288107. Unknown parameter |month= ignored (help); replacement character in |pages= at position 4 (help)
  3. Template:WhoNamedIt
  4. Goto M, Rubenstein M, Weber J, Woods K, Drayna D (1992). "Genetic linkage of Werner's syndrome to five markers on chromosome 8". Nature. 355 (6362): 735–8. doi:10.1038/355735a0. PMID 1741060. Unknown parameter |month= ignored (help)
  5. 5.0 5.1 Leistritz, F. NCBI. Werner Syndrome. Retrieved Jun 2, 2011, from http://www.ncbi.nlm.nih.gov/books/NBK1514/