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A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome
Noonan syndrome (NS) is an autosomal dominant disorder in some cases caused by PTPN11 mutations. Since somatic mutations in PTPN11 are seen in several tumor types, NS which causes germline PTPN11 mutations are also increase the risk of hematologic malignancies and brain solid tumors. However, the re...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766114/ https://www.ncbi.nlm.nih.gov/pubmed/31637070 http://dx.doi.org/10.1155/2019/6091059 |