Case of Stickler syndrome in a child without retinal detachment

African Vision and Eye Health

 
 
Field Value
 
Title Case of Stickler syndrome in a child without retinal detachment
 
Creator Hampango, Moono Wei, Jing Xia, Yifan
 
Subject Ophthalmology; Optometry COL2A1 gene; stickler syndrome Type I; high myopia; exome sequencing; retinal degeneration
Description Introduction: Stickler syndrome is a rare form of hereditary generalised collagenopathies that manifests as ocular, skeletal, auditory and orofacial symptoms. It arises because of mutations in the procollagen genes COL2A1, COL9A1, COL9A2, COL9A3, COL11A1 and COL11A2.Patient presentation: An 11-year-old Chinese boy was referred to our hospital with a history of reduced and distorted vision. He had a history of amblyopia and high myopia by age 4 years. A comprehensive medical assessment was conducted which included complete systemic, ophthalmic, optometric examinations and genetic testing. The patient had characteristic signs of Stickler syndrome which include high myopia, a cataract, open-angle glaucoma, anterior high iris root insertion, membranous vitreous changes, peripheral retinal degeneration and foveal hypoplasia but no retinal detachment. No obvious auditory, orofacial, or skeletal abnormalities were found. Exome sequencing identified COL2A1 heterozygous splicing variation. He is a child of nonrelated parents. His mother is highly myopic.Management and outcome: After optometry assessment, amblyopia and myopia were corrected. Glaucoma medication was given, and retinal laser photocoagulation was performed. The patient’s vision is currently stable.Conclusion: COL2A1 gene pathogenic splicing mutation was discovered in a Stickler syndrome type I patient with an ocular-only manifestation. Exome sequencing results indicated site c.1597CT/p. Arg533*(NM_001844.5) which is a heterozygous variant inherited from the mother.Contribution: In this report, we demonstrate how clinical presentation and molecular genetic tests are helpful in making the diagnosis of Stickler syndrome before retinal detachment.
 
Publisher AOSIS
 
Contributor Nil
Date 2024-07-18
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — Case report
Format text/html application/epub+zip text/xml application/pdf
Identifier 10.4102/aveh.v83i1.876
 
Source African Vision and Eye Health; Vol 83, No 1 (2024); 7 pages 2410-1516 2413-3183
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://avehjournal.org/index.php/aveh/article/view/876/2484 https://avehjournal.org/index.php/aveh/article/view/876/2485 https://avehjournal.org/index.php/aveh/article/view/876/2486 https://avehjournal.org/index.php/aveh/article/view/876/2487
 
Coverage China; Henan province 2022 - 2023 11 year old boy
Rights Copyright (c) 2024 Moono Hampango, Jing Wei, Yifan Xia https://creativecommons.org/licenses/by/4.0
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