New PTEN mutation identified in a patient with rare bilateral choroidal ganglioneuroma
Abstract Background Choroidal ganglioneuroma is an extremely rare tumor, and there is little knowledge regarding its pathogenesis. We aimed to investigate the phenotypic and genetic alterations in one sporadic patient with a rare case of bilateral choroidal ganglioneuroma. Methods A 6-year-old boy w...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMC
2020-12-01
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| Edice: | BMC Ophthalmology |
| Témata: | |
| On-line přístup: | https://doi.org/10.1186/s12886-020-01760-y |
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