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Common Somatic Alterations Identified in Maffucci Syndrome by Molecular Karyotyping
Maffucci syndrome (MS) is a rare congenital disorder characterized by multiple central cartilaginous tumors (enchondromas) in association with cutaneous spindle cell hemangiomas. These patients have a high incidence of malignant transformation. No familial case is known and the etiopathogenic cause...
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| Veröffentlicht in: | Mol Syndromol |
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| Hauptverfasser: | , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
S. Karger AG
2014
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4281579/ https://ncbi.nlm.nih.gov/pubmed/25565925 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000365898 |
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