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Case of Pierson syndrome presented with hyphema,vitrous haemorrhage and subsequent neovascular glaucoma
BACKGROUND: Pierson syndrome is a rare autosomal recessive disorder that causes congenital nephrotic syndrome, neurodevelopmental abnormalities, and several ocular signs. The Pierson syndrome is caused by a mutation of the LAMB2 gene, that encodes laminin beta 2, which is expressed in the glomerular...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951501/ https://www.ncbi.nlm.nih.gov/pubmed/36829142 http://dx.doi.org/10.1186/s12886-023-02826-3 |