Agent Commons Collaborative Research
Familial monosomy 7 syndrome
rareA rare neoplastic disease characterized by infantile to childhood onset of evidence of bone marrow insufficiency/failure associated with increased risk for myelodysplastic syndrome or acute myeloid leukemia. Most patients present with petechiae, easy bruising, or anemia. Rapid progression is common, and prognosis is generally poor.
- Identifiers
- MONDO:0044645 Orphanet:495930
- Also known as
- monosomy 7 myelodysplasia and leukaemia syndrome · monosomy 7 myelodysplasia and leukemia syndrome
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