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Hereditary recurrent myoglobinuria

MONDO:0020504

An inborn error of metabolism characterized by abnormal urinary excretion of myoglobin due to acute destruction of skeletal muscle fibers.

Also known as: genetic recurrent myoglobinuria

1 clinical trial for this condition and its sub-types, 0 tagged with Hereditary recurrent myoglobinuria itself.

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↑ Inborn errors of metabolism (2231)

Sub-types of Hereditary recurrent myoglobinuria

Myoglobinuria, acute recurrent, autosomal recessive 1 trial
Myoglobinuria, recurrent 0 trials

Including sub-types (1) Tagged with Hereditary recurrent myoglobinuria (0)

Exercise test could revolutionize monitoring of rare metabolic muscle disease

Knowledge-focused Completed

This study looked at whether an exercise test can be used to monitor patients with a rare hereditary disease that causes severe muscle breakdown (rhabdomyolysis). Researchers measured heart function and oxygen use during exercise in 27 patients. The goal was to find a reliable wa…

Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused

Last updated Jun 26, 2026 16:02 UTC