The international X-linked hypophosphataemia (XLH) registry (NCT03193476): rationale for and description of an international, observational study | Orphanet Journal of Rare Diseases | Full Text

The international X-linked hypophosphataemia (XLH) registry (NCT03193476): rationale for and description of an international, observational study | Orphanet Journal of Rare Diseases | Full Text

The international X-linked hypophosphataemia (XLH) registry (NCT03193476): rationale for and description of an international, observational study

X-linked hypophosphataemia (XLH) is a rare, hereditary, progressive and lifelong phosphate wasting disorder characterised by pathological elevations in fibroblast growth factor (FGF) 23 concentration and activ...

Authors:Raja Padidela, Ola Nilsson, Outi Makitie, Signe Beck-Nielsen, Gema Ariceta, Dirk Schnabel, Maria Luisa Brandi, Annemieke Boot, Elena Levtchenko, Michael Smyth, Ravi Jandhyala and Zulf Mughal

Citation:Orphanet Journal of Rare Diseases 2020 15:172

Content type:Research

 

Published on: 30 June 2020

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