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Maffucci syndrome
rareMaffucci syndrome is a very rare genetic bone and skin disorder characterized by multiple enchondromas, leading to bone deformities, combined with multiple dark, irregularly shaped hemangiomas or less commonly lymphangiomas.
- Identifiers
- MONDO:0013808 OMIM:614569Orphanet:163634
- Part of
- Developmental defect during embryogenesisHereditary disorder of connective tissueHereditary neoplastic syndromeHereditary skin disorderOvergrowth syndromeSkin neoplasmSkin vascular diseaseVascular bone neoplasm
- Also known as
- chondrodysplasia with hemangioma · Chondroplasia angiomatosis · Dyschondrodysplasia with hemangiomas · Dyschondroplasia and cavernous hemangioma · enchondromatosis with hemangiomata
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