First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review

First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review

Abstract Background Severe congenital ophthalmological malformations and glaucoma might be an important occasional feature in patients with Coffin-Siris syndrome (CSS), especially Coffin-Siris syndrome 9 (CSS9, OMIM #615866) caused by SOX11 mutation. Recently, primary (open-angle) glaucoma was descr...

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Bibliographic Details
Main Authors: Heidi Diel, Can Ding, Franz Grehn, Panagiotis Chronopoulos, Oliver Bartsch, Esther M. Hoffmann
Format: Article
Language:English
Published: BMC 2021-01-01
Series:BMC Ophthalmology
Subjects:
Coffin-Siris syndrome
Coffin-Siris syndrome 9
SOX11 gene
Secondary childhood glaucoma
Anterior segment dysgenesis
Peters anomaly
Online Access:https://doi.org/10.1186/s12886-020-01788-0

Internet

https://doi.org/10.1186/s12886-020-01788-0

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