OSLAM syndrome (Q7073028)
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OSLAM syndrome is characterised by the association of osteosarcoma, limb anomalies (clinodactyly with brachymesophalangy, bilateral radioulnar synostosis and absence of one digital ray of the foot) and red cell macrocytosis without anaemia
- Osteosarcoma - limb anomalies - erythroid macrocytosis
- Osteosarcoma, Limb Anomalies, and Macrocytosis
- OSLAM SYNDROME
- Osteosarcoma-limb anomalies-erythroid macrocytosis syndrome
- Osteosarcoma, Limb Anomalies, and Erythroid Macrocytosis With Megaloblastic Marrow
Language | Label | Description | Also known as |
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English | OSLAM syndrome |
OSLAM syndrome is characterised by the association of osteosarcoma, limb anomalies (clinodactyly with brachymesophalangy, bilateral radioulnar synostosis and absence of one digital ray of the foot) and red cell macrocytosis without anaemia |
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Wikipedia(3 entries)
- arwiki متلازمة أوسلام
- enwiki OSLAM syndrome
- fiwiki OSLAM-oireyhtymä