Medulloblastoma and Cowden Syndrome: Further Evidence of an Association
Cowden syndrome (CS) is an autosomal dominant hamartoma and tumor predisposition syndrome caused by heterozygous pathogenic germline variants in PTEN in most affected individuals. Major features include macrocrania, multiple facial tricholemmomas, acral and oral keratoses and papillomas, as well as...
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| Auteurs principaux: | , , , , , , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
University of Münster / Open Journals System
2022-01-01
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| Collection: | Free Neuropathology |
| Sujets: | |
| Accès en ligne: | https://www.uni-muenster.de/Ejournals/index.php/fnp/article/view/3684 |
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