BIOTINIDASE DEFICIENCY

Clinical trials for BIOTINIDASE DEFICIENCY explained in plain language.

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Researchers track rare disorder in kids to unlock genetic clues

Knowledge-focused Recruiting now

This study aims to better understand biotinidase deficiency, a rare inherited disorder, in children identified through newborn screening in Italy. Researchers will follow about 180 children for at least three years to see how their specific genetic changes relate to their symptom…

Matched conditions: BIOTINIDASE DEFICIENCY

Sponsor: IRCCS Azienda Ospedaliero-Universitaria di Bologna • Aim: Knowledge-focused

Last updated Mar 27, 2026 12:40 UTC

BIOTINIDASE DEFICIENCY

Get alerted when new BIOTINIDASE DEFICIENCY trials appear

Researchers track rare disorder in kids to unlock genetic clues