Indication
Myelodysplastic syndrome
Myelodysplastic syndrome refers to a heterogeneous group of clonal hematopoietic stem cell neoplasms characterized by ineffective hematopoiesis, progressive peripheral blood cytopenias, and morphologic dysplasia across one or more blood cell lineages. Read more about Myelodysplastic syndrome
45 drugs 37 manufacturers
Drugs that treat it
Common Myelodysplastic syndrome therapies.
DECITABINE
AZACITIDINE
AZACITIDINE
DECITABINE
DECITABINE
AZACITIDINE
AZACITIDINE
DECITABINE
News & literature
Coming soonRelated codes
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Coming soonMyelodysplastic syndrome refers to a heterogeneous group of clonal hematopoietic stem cell neoplasms characterized by ineffective hematopoiesis, progressive peripheral blood cytopenias, and morphologic dysplasia across one or more blood cell lineages.
Primarily affecting older adults, this hematologic disorder arises from acquired genetic or cytogenetic abnormalities within bone marrow progenitor cells that impair cellular maturation and survival.
Patients frequently present with fatigue, recurrent infections, or bleeding secondary to profound anemia, neutropenia, or thrombocytopenia.
Clinically, the syndrome exhibits variable risk of disease progression, carrying a substantial potential to transform into acute myeloid leukemia.
- nih.gov
Myelodysplastic syndrome refers to a heterogeneous group of clonal hematopoietic stem cell neoplasms characterized by ineffective hematopoiesis, progressive peripheral blood cytopenias, and morphologic dysplasia across one or more blood cell lineages Primarily affecting older adults, this hematologic disorder arises from acquired genetic or cytogenetic abnormalities within bone marrow progenitor cells that impair cellular maturation and survival Clinically, the syndrome exhibits variable risk of...
- nih.gov
Myelodysplastic syndrome refers to a heterogeneous group of clonal hematopoietic stem cell neoplasms characterized by ineffective hematopoiesis, progressive peripheral blood cytopenias, and morphologic dysplasia across one or more blood cell lineages Primarily affecting older adults, this hematologic disorder arises from acquired genetic or cytogenetic abnormalities within bone marrow progenitor cells that impair cellular maturation and survival Patients frequently present with fatigue, recurren...
- medlineplus.gov
Clinically, the syndrome exhibits variable risk of disease progression, carrying a substantial potential to transform into acute myeloid leukemia
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