Myopathy, lactic acidosis, and sideroblastic anemia

MONDO:0000863

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.

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Sub-types

Myopathy, lactic acidosis, and sideroblastic anemia 1 (0) Myopathy, lactic acidosis, and sideroblastic anemia 2 (0) Myopathy, lactic acidosis, and sideroblastic anemia 3 (0)

Broader categories

Disease (680) Anemia (233) Metabolic disease (233) Musculoskeletal system disorder (207) Hereditary disease (176) Hematologic disorder (170) Inborn mitochondrial metabolism disorder (58) Muscle tissue disorder (56) Inborn errors of metabolism (45) Mitochondrial disease (40)

Trials to join now! 14 Not yet recruiting 3 Not yet finished but already full! 6 Completed 4 Terminated 1

Myopathy, lactic acidosis, and sideroblastic anemia

Sub-types

Broader categories

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