Panel Discussion: Some Aspects of the Management of Patients with X-Linked Hypophosphataemic Rickets

Adv Ther. 2020 May;37(Suppl 2):121-126. doi: 10.1007/s12325-019-01208-w. Epub 2020 Mar 31.

Abstract

X-linked hypophosphataemia (XLH) rickets is a rare disease frequently misdiagnosed and mismanaged. Despite having clinical guidelines that offers some therapeutic recommendations based on the clinical experience of experts, physicians still have questions about some important aspects of the diagnosis and treatment of XLH, such as when the disease should be suspected, who should be in charge of the diagnosis, what should be done once the disease is diagnosed, or what therapeutic options are currently available. The objective of this paper is to answer some of the more frequent questions related to the management of patients with XLH by a group of experts participating in a scientific conference on XLH held in Madrid.

Keywords: Burosumab; Diagnosis; FGF23; Multidisciplinary; Orthopaedics; Paediatrician; Phosphaturia.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adolescent
  • Antibodies, Monoclonal / therapeutic use*
  • Child
  • Child, Preschool
  • Drug Dosage Calculations
  • Drug Therapy / standards*
  • Familial Hypophosphatemic Rickets / diagnosis*
  • Familial Hypophosphatemic Rickets / drug therapy*
  • Female
  • Fibroblast Growth Factor-23
  • Humans
  • Male
  • Practice Guidelines as Topic*

Substances

  • Antibodies, Monoclonal
  • FGF23 protein, human
  • Fibroblast Growth Factor-23