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Myopathy, lactic acidosis, and sideroblastic anemia
rareMitochondrial myopathy and sideroblastic anemia belongs to the heterogeneous family of metabolic myopathies. It is characterized by progressive exercise intolerance manifesting in childhood, onset of sideroblastic anemia around adolescence, lactic acidaemia, and mitochondrial myopathy.
- Identifiers
- MONDO:0000863 Orphanet:2598
- Part of
- Congenital anemiaInborn mitochondrial myopathyInherited sideroblastic anemiaMitochondrial oxidative phosphorylation disorder
- Also known as
- mitochondrial myopathy and sideroblastic anaemia · mitochondrial myopathy and sideroblastic anemia · MLASA · MSA · myopathy with lactic acidosis and sideroblastic anaemia
Subtypes
Rare disease
Projects
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