Myopathy, lactic acidosis, and sideroblastic anemia

Mitochondrial 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.

Also known as: MLASA, MSA, mitochondrial myopathy and sideroblastic anaemia, mitochondrial myopathy and sideroblastic anemia, myopathy, lactic acidosis and sideroblastic anaemia, myopathy, lactic acidosis and sideroblastic anemia, myopathy, lactic acidosis, and siderblastic anaemia, myopathy, lactic acidosis, and siderblastic anemia

28 clinical trials for this condition and its sub-types.