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Sideroblastic anemia
MONDO:0015194A group of rare heterogeneous inherited or acquired bone marrow disorders, isolated or part of a syndrome, characterized by decreased hemoglobin synthesis, because of defective use of iron (although plasmatic iron levels may be normal or elevated) and the presence of ringed sideroblasts in the bone marrow due to the pathologic iron overload in mitochondria as visualized by Perls' staining. The group encompasses (idiopathic) acquired sideroblastic anemia and constitutional sideroblastic anemias. The latter include syndromic sideroblastic anemias such as Pearson syndrome, mitochondrial mypathy and sideroblastic anemias, x-linked sideroblastic anemia-ataxia, thiamine responsive megaloblastic anemia syndrome and nonsyndromic sideroblastic anemias comprising x-linked and autosomal recessive sideroblastic anemias.
Also known as: anaemia sideroblastic, anemia sideroblastic, sideroblastic anemia
23 clinical trials for this condition and its sub-types, 0 tagged with Sideroblastic anemia itself.
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Sub-types of Sideroblastic anemia
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Inherited sideroblastic anemia 2 trials · 7 incl. sub-types
8 sub-types
- Myopathy, lactic acidosis, and sideroblastic anemia 3 trials Sub-types →
- Autosomal recessive sideroblastic anemia 2 trials Sub-types →
- X-linked sideroblastic anemia 1 0 trials
- X-linked sideroblastic anemia with ataxia 0 trials
- Anemia, sideroblastic, 5 0 trials
- Autosomal dominant sideroblastic anemia 0 trials
- Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome 0 trials
- Severe congenital hypochromic anemia with ringed sideroblasts 0 trials
Most studied deeper sub-types
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