Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Mitochondrial disease · Inherited sideroblastic anemia · X-linked cerebellar ataxia
X-linked sideroblastic anemia with ataxia
A rare syndromic, inherited form of sideroblastic anemia in which the cause of the disease is a mutation in the ABCB7 gene and is characterized by mild to moderate anemia (with hypochromia and microcytosis) and early-onset, non- or slowly progressive spinocerebellar ataxia.
This condition has no sub-types.