Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory.

Orphanet J Rare Dis · 2026 · PMC12964787 · PMID 41639888

Europe PMC DOI

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closest p

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did not reach statistical significanceno p-value reported

As the primary endpoint did not reach statistical significance, all key secondary and secondary endpoints are reported with nominal p-values, which should thus be interpreted with caution.

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