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Barth syndrome

Barth syndrome

Human genetic metabolism disorder.

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Readers' pathsAug 2026 – Oct 2026

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  1. Elamipretide

    Chemical compound.

    42%

  2. Neutropenia

    Abnormally low concentration of neutrophils (a type of white blood cell) in the blood.

    17%

  3. Cardiomyopathy

    Disease of the heart muscle.

    11%

  4. 3-Methylglutaconic aciduria

    Medical condition.

    9.6%

  5. Tafazzin

    Protein found in humans.

    4.9%

  6. Exercise intolerance

    Inability to perform physical exercise at normal levels.

    2.9%

Readers come from

Share of the 695 readers arriving from another article

  1. Elamipretide

    Chemical compound.

    56%

  2. Neutropenia

    Abnormally low concentration of neutrophils (a type of white blood cell) in the blood.

    9.2%

  3. Mitochondrial myopathy

    Muscle disorders caused by mitochondrial dysfunction.

    2%

  4. X-linked recessive inheritance

    Mode of inheritance.

    1.9%

  5. Mitochondria

    Organelle in eukaryotic cells responsible for respiration.

    1.6%

  6. Microlissencephaly

    Microcephaly combined with lissencephaly.

    1.4%

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