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Knobloch syndrome associated with Polymicrogyria and early onset of retinal detachment: two case reports
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 abnormalities are...
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| Pubblicato in: | BMC Ophthalmol |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5702215/ https://ncbi.nlm.nih.gov/pubmed/29178892 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12886-017-0615-z |
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