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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Detalles Bibliográficos
Autores principales: White, Robert J., Wang, Yao, Tang, Peter, Montezuma, Sandra R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
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

Internet

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

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