Role of fibroblast growth factor-23 as an early marker of metabolic bone disease of prematurity.
Sandra Llorente-PelayoPablo DocioSilvia ArriolaBernardo Alio Lavin-GomezMaria Teresa García UnzuetaMaría Ángeles BallesterosMaría J Cabero-PérezDomingo González-LamuñoPublished in: BMC pediatrics (2024)
MBDP remains a significant concern in extremely premature newborns. Current diagnostic methods rely on limited biochemical markers. Early detection of low FGF23 levels enables timely interventions, potentially averting demineralization.