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X-linked sideroblastic anemia with ataxia

MONDO:0010524

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.

Also known as: ASAT, Pagon-Bird-Detter syndrome, X-linked sideroblastic anaemia with spinocerebellar ataxia, X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with spinocerebellar ataxia, XLSA-A, anaemia sideroblastic and spinocerebellar ataxia, anemia, sideroblastic, with ataxia, X-linked recessive

40 clinical trials for this condition and its sub-types, 0 tagged with X-linked sideroblastic anemia with ataxia itself.

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