Familial monosomy 7 syndrome

A 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.

Also known as: monosomy 7 myelodysplasia and leukaemia syndrome, monosomy 7 myelodysplasia and leukemia syndrome

1576 clinical trials for this condition and its sub-types, 0 tagged with Familial monosomy 7 syndrome itself.