Ectopia Lentis with Retinal Detachment in a Patient with Marfan Syndrome: A Case Report
Marfan syndrome is an autosomal dominant hereditary connective tissue disease caused by mutations in the Fibrillin-1 gene located on chromosome 15q15-21. Fibrillin is a specific type of glycoprotein widely distributed throughout the body, contributing to the elasticity and load-bearing capacity of c...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
JCDR Research and Publications Private Limited
2024-04-01
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| Series: | Journal of Clinical and Diagnostic Research |
| Subjects: | |
| Online Access: | https://www.jcdr.net/articles/PDF/19220/66942_CE[Ra1]_F(SS)_QC(PS_RDW_IS)_PF1(VD_DK_OM)_PFA(VD_KM)_PN(KM).pdf |