Prevention of Blindness in Stickler Syndrome.
MetadataShow full item record
Alexander, P., & Snead, M. (2022). Prevention of Blindness in Stickler Syndrome.. Genes (Basel), 13 (7), 1150-1150. https://doi.org/10.3390/genes13071150
Stickler syndromes are inherited conditions caused by abnormalities of structural proteins in the eye, inner ear and cartilage. The risk of retinal detachment, particularly due to the development of giant retinal tears, is high. Stickler syndrome is the most common cause of childhood retinal detachment. Although retinal detachment surgery in the general population has a high success rate, outcomes from surgical repair in Stickler syndrome patients are notoriously poor, providing a strong argument for prophylactic intervention. Variable case selection, absence of molecular genetic sub-typing and inconsistent treatment strategies have all contributed to the historic uncertainty regarding the safety and efficacy of prophylactic treatment. This paper reviews the major published clinical studies that have evaluated different methods and strategies for prophylaxis. Based on the current body of literature, there is extremely strong evidence from cohort comparison studies demonstrating the efficacy and safety of prophylactic retinopexy to reduce, but not eliminate, the risk of retinal detachment in Stickler syndrome patients. It is vital that this body of evidence is provided to Stickler syndrome patients, to enable them to make their own fully informed choice about whether to receive prophylaxis for themselves and particularly on behalf of their affected children, to reduce the risk of retinal detachment.
External DOI: https://doi.org/10.3390/genes13071150
This record's URL: https://www.repository.cam.ac.uk/handle/1810/339020
Attribution 4.0 International
Licence URL: https://creativecommons.org/licenses/by/4.0/