eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | marfan syndrome |
| Comorbidity | C0023316|lens subluxation |
| Sentences | 6 |
| PubMedID- 24138040 | Gene mutations have been identified for lens subluxation associated with marfan syndrome, weill marchesani syndrome, ectopia lentis simplex, ectopia lentis et pupillae, ehlers danlos syndrome, homocystinuria, and sulfite oxidase deficiency. |
| PubMedID- 24348399 | During the surgery, there were no specific findings of cystic medial necrosis or crystalline lens subluxation due to the marfan syndrome. |
| PubMedID- 24698610 | Surgical management of lens subluxation in marfan syndrome. |
| PubMedID- 24698609 | Background: autosomal dominant mutation of the fbn1 gene (fibrillin-1) results in a spectrum of disease (type 1 fibrillopathies) ranging from marfan syndrome with lens subluxation and cardiovascular complications to milder connective tissues phenotypes. |
| PubMedID- 21668788 | Comparison of clinical outcomes between iris-fixated anterior chamber intraocular lenses and scleral-fixated posterior chamber intraocular lenses in marfan syndrome with lens subluxation. |
| PubMedID- 22949916 | The primary indications for the ring were found to be as mature cataract, traumatic cataract, pseudoexfoliation syndrome and lens subluxation due to marfan syndrome. |
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