Review
doi: 10.1007/978-3-031-72230-1_42.
Stickler Syndrome
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- PMID: 40736844
- DOI: 10.1007/978-3-031-72230-1_42
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Review
Stickler Syndrome
Adv Exp Med Biol.
2025.
Abstract
Stickler syndrome represents the most common hereditary hyaloideoretinopathy caused by mutations affecting various types of collagen which make up the vitreous as well as cartilage and other connective tissues.
© 2025. The Author(s), under exclusive license to Springer Nature Switzerland AG.
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References
Further Reading
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- Genes (Basel). 2022; 13(6): 1089.
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- Eye. 1996;10:701–708.
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- Eye (Lond). 2022 Oct;36(10): 1966–1972.
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- Clin Ophthalmol. 2016; 10: 1531–1534.
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- Retina 43(1):p 88-93, January 2023.
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