ALKAPTONURIA

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Rare disease study aims to unlock secrets of alkaptonuria

Knowledge-focused Recruiting now

This study aims to better understand alkaptonuria, a rare genetic disease that causes a pigment to build up in bones and tissues, leading to arthritis, fractures, and other problems. Researchers will evaluate 300 patients aged 2 and older every 2 to 3 years using modern medical t…

Matched conditions: ALKAPTONURIA

Sponsor: National Human Genome Research Institute (NHGRI) • Aim: Knowledge-focused

Last updated May 26, 2026 06:24 UTC

ALKAPTONURIA

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Rare disease study aims to unlock secrets of alkaptonuria