ehlers_danlos_syndrome

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ehlers_danlos_syndrome [2024/04/11 14:24] oculomanehlers_danlos_syndrome [2024/04/11 14:44] (current) oculoman
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 ====Main Features==== ====Main Features====
-  * Group of heritable connective tissue disorderes+  * Group of heritable connective tissue disorders
   * tissue fragility    * tissue fragility 
   * hypermobility   * hypermobility
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     * convergence insufficiency      * convergence insufficiency 
   * lenticular changes   * lenticular changes
-    * Ectopia lentos+    * Ectopia lentis
   * Blue sclerae    * Blue sclerae 
   * conjunctivochalasis    * conjunctivochalasis 
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   * Gene defect involving collagen   * Gene defect involving collagen
     * usually collagen types I, III, and V     * usually collagen types I, III, and V
-    * 13 subtypes proposed by the Ehlers-Danlos Syndrome International Symposium in 2016+    * {{::the_2017_international_classification_of_the_ehlers_danlos_syndromes.pdf |Ehlers-Danlos Syndrome International Classification 2017}}
     * Disruption of the collagen fibrils      * Disruption of the collagen fibrils 
     * Classical EDS     * Classical EDS
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   * Loeys-Deitz syndrome   * Loeys-Deitz syndrome
 ====Reference==== ====Reference====
-  * [[EyeWiki|https://eyewiki.aao.org/Ehlers-Danlos_Syndrome] +[[https://eyewiki.aao.org/Ehlers-Danlos_Syndrome|EyeWiki]]\\ 
-  [[linkSingman EL, Doyle JJ. Angioid Streaks Are Not a Common Feature of Ehlers-Danlos Syndrome. JAMA Ophthalmol. 2019;137(3):239.]]+[[https://jamanetwork-com.proxy.lib.uiowa.edu/journals/jamaophthalmology/fullarticle/2717493Singman | EL, Doyle JJ. Angioid Streaks Are Not a Common Feature of Ehlers-Danlos Syndrome. JAMA Ophthalmol. 2019;137(3):239.]]\\ 
 +{{:the_2017_international_classification_of_the_ehlers_danlos_syndromes.pdf |2017 International Classification}}
  
 {{tag>syndrome}} {{tag>syndrome}}
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