Genotype-phenotype Correlations of Ocular Posterior Segment Abnormalities in Marfan Syndrome
Purpose: Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in the fibrillin-1 ( (FBN1). In addition to typical phenotypes such as ectopia lentis (EL) and aortic dilation, patients with MFS are prone to ocular posterior segment abnormalities, including retinal detachment (RD),...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Elsevier
2024-09-01
|
| Sarja: | Ophthalmology Science |
| Aiheet: | |
| Linkit: | http://www.sciencedirect.com/science/article/pii/S2666914524000629 |
| Tagit: |
Ei tageja, Lisää ensimmäinen tagi!
|