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Myoglobinuria, acute recurrent, autosomal recessive

MONDO:0009992

Also known as: myoglobinuria, acute recurrent, autosomal recessive, myoglobinuria, familial paroxysmal paralytic, rhabdomyolysis, acute recurrent

1 clinical trial for this condition and its sub-types, 1 tagged with Myoglobinuria, acute recurrent, autosomal recessive itself.

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↑ Acute disease (4756) ↑ Hereditary recurrent myoglobinuria (1)

Including sub-types (1) Tagged with Myoglobinuria, acute recurrent, autosomal recessive (1)

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