====== Ectopia Lentis ======
===== Genetics =====
^ Condition                            ^ Inheritance Pattern  ^ Gene      ^
| [[marfan_syndrome|Marfan Syndrome]]  | Autosomal Dominant   | FBN1      |
| Simple Ectopia Lentis                | Autosomal Dominant   | FBN1      |
| [[ehlers_danlos_syndrome|Ehlers-Danlos Syndrome]] (classical type)| Autosomal Dominant |COL5A1 and COL5A2|
| Homocystinuria                       | Autosomal Recessive  | CS        |
| Weill-Marchesani Syndrome            | Autosomal Recessive  | ADAMTS10  |
| WM-like Syndrome                     | Autosomal Recessive  | ADAMTS17  |
| Knoblock syndrome                    | Autosomal Recessive  | COL18A1   |
| Cohen Syndrome                       | Autosomal Recessive  | COH1      |
| Megalocornea with ectopia lentis     | Autosomal Recessive  | LTBP2     |
| Ectopia lentis et pupillae           | Autosomal Recessive  | ADAMTSL4  |
| Ectopia lentis with filtering blebs  | Autosomal Recessive  | ASPH      |

  * Adapted from: [[https://my.clevelandclinic.org/staff/2272-elias-traboulsi|Elias Traboulsi,MD,M.Ed]]  University of Iowa Research Day Keynote Speaker 4/21/2017

{{tag>syndrome}}