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Treatment of cystoid macular edema in homozygous twins with glutathione synthetase deficiency and retinal dystrophy.
Author: ConrathJ, DonnadieuB, FakhouryO, MatontiF, WarrakR
Original Abstract of the Article :
Monozygotic twins with glutathione synthetase deficiency, progressive retinal dystrophy and cystoid macular edema were followed for foveal changes on optical coherence tomography under different treatment modalities. The purpose of the study is to show the effect of topical dorzolamide in conjunctio...See full text at original site
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引用元:
https://doi.org/10.1016/j.jfo.2017.08.010
データ提供:米国国立医学図書館(NLM)
Cystoid Macular Edema: A Case Study of Glutathione Synthetase Deficiency
The human eye is a delicate and intricate organ, responsible for sight and perception. This case study delves into the complexities of cystoid macular edema (CME), a condition characterized by fluid accumulation in the macula, a central region of the retina essential for sharp vision. This particular case study focuses on two homozygous twins with glutathione synthetase deficiency (GSSD), a rare genetic disorder that can lead to retinal dystrophy and CME.
The researchers followed the twins for foveal changes on optical coherence tomography (OCT) under different treatment modalities. They found that both systemic acetazolamide and topical dorzolamide, medications used to reduce fluid buildup in the eye, were effective in decreasing CME in both patients. The effect was temporary but provided relief for a certain period.
A Glimpse Into GSSD: Understanding the Challenge of Rare Disorders
This case study provides valuable insights into the challenges of treating CME in patients with GSSD, a rare genetic disorder. The researchers' findings offer a potential treatment approach, but emphasize the need for further research to explore the long-term effectiveness and safety of these medications.
Navigating Eye Health: The Importance of Early Detection and Treatment
This case study underscores the importance of early detection and treatment for eye conditions like CME, particularly in individuals with rare genetic disorders. Prompt medical attention and personalized treatment strategies can help preserve vision and improve quality of life.
Dr. Camel's Conclusion
This case study provides a detailed account of treating CME in homozygous twins with GSSD, highlighting the challenges of managing rare disorders. It offers valuable insights into potential treatment strategies but emphasizes the need for further research to improve our understanding and management of this complex condition.
Date :
- Date Completed 2018-09-24
- Date Revised 2018-09-24
Further Info :
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