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PREVALENCE, RISK FACTORS, AND OUTCOMES OF RHEGMATOGENOUS RETINAL DETACHMENTS REPAIR IN MARFAN SYNDROME
Ahmed A Nagshbandi1,2, Moustafa S Magliyah1, Abdulrahman F Algwaiz1
1Vitreoretinal Division, King Khalid Eye Specialist Hospital, Riyadh, Saudi Arabia.
Purpose:
To report the prevalence, risk factors, and surgical management outcomes of rhegmatogenous retinal detachment (RRD) in Marfan syndrome.
Methods:
Retrospective chart review of 82 patients with Marfan syndrome who have developed RRD. The collected data included lens status, previous surgeries, details of intraoperative retinal findings, and follow-up outcomes.
Results:
The study included 163 eyes of 82 patients. Forty-three patients (52.4%) were males. The mean duration of follow-ups was 15.3 ± 13.4 years. RRD occurred in 54 eyes (33.1%). The mean age at the time of RRD was 25.2 ±12.5 years. Risk of RRD was significantly higher among patients who had previous trauma ( P = 0.014), previous ocular surgery ( P = 0.001), lensectomy without implantation of an intraocular lens ( P = 0.002), aphakia ( P < 0.001), lens subluxation ( P = 0.002), and higher axial length ( P < 0.001). Successful primary reattachment was achieved in 36 eyes (69.2%), whereas 16 eyes (30.8%) required secondary repairs to achieve reattachments.
Conclusion:
Eyes with Marfan syndrome have a 33.1% risk of developing RRD upon long-term follow-ups. Previous trauma, intraocular surgeries, aphakic status, and high axial length are associated with higher risk. High reattachments rates could be achieved after surgical repairs.
Insights
Patients with Marfan Syndrome face a 33.1% risk of rhegmatogenous retinal detachment (RRD). Factors like trauma, ocular surgery, aphakia, and longer axial length increase this risk, but surgical repair offers high reattachment rates.
Area of Science:
- Ophthalmology
- Genetics
- Retinal Surgery
Background:
- Marfan Syndrome is a genetic disorder affecting connective tissue.
- Retinal detachment is a known complication, but its prevalence and risk factors in Marfan Syndrome require further elucidation.
Purpose of the Study:
- To determine the prevalence of rhegmatogenous retinal detachment (RRD) in patients with Marfan Syndrome.
- To identify risk factors associated with RRD development in this population.
- To evaluate the outcomes of surgical management for RRD in Marfan Syndrome patients.
Main Methods:
- Retrospective chart review of 82 patients diagnosed with Marfan Syndrome and RRD.
- Data collection included lens status, prior ocular surgeries, intraoperative findings, and follow-up outcomes.
- Analysis focused on identifying statistically significant risk factors and surgical success rates.
Main Results:
- Rhegmatogenous retinal detachment (RRD) occurred in 33.1% of eyes (54 out of 163) in the study cohort.
- Significant risk factors for RRD included prior trauma, previous ocular surgery, lensectomy without intraocular lens implantation, aphakia, lens subluxation, and increased axial length.
- Successful primary reattachment was achieved in 69.2% of eyes, with secondary repairs achieving reattachment in the remaining cases.
Conclusions:
- Eyes with Marfan Syndrome have a substantial lifetime risk (33.1%) of developing RRD.
- Specific factors such as trauma, ocular surgeries, aphakia, and high axial length are strongly associated with an increased risk of RRD.
- Surgical intervention for RRD in Marfan Syndrome patients can achieve high rates of successful retinal reattachment.
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