Knobloch syndrome associated with Polymicrogyria and early onset of retinal detachment: two case reports

Abstract Background Knobloch Syndrome (KS) is a rare congenital syndrome characterized by occipital skull defects and vitreoretinal degeneration. Retinal detachment (RD) often occurs at the end of the first decade of life or later. Aside from occipital skull defects, central nervous system abnormali...

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Bibliographic Details
Main Authors: Robert J. White, Yao Wang, Peter Tang, Sandra R. Montezuma
Format: Article
Language:English
Published: BMC 2017-11-01
Series:BMC Ophthalmology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12886-017-0615-z

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