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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702215/ https://www.ncbi.nlm.nih.gov/pubmed/29178892 http://dx.doi.org/10.1186/s12886-017-0615-z |