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Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia.
Haffner, Dieter; Emma, Francesco; Eastwood, Deborah M; Duplan, Martin Biosse; Bacchetta, Justine; Schnabel, Dirk; Wicart, Philippe; Bockenhauer, Detlef; Santos, Fernando; Levtchenko, Elena; Harvengt, Pol; Kirchhoff, Martha; Di Rocco, Federico; Chaussain, Catherine; Brandi, Maria Louisa; Savendahl, Lars; Briot, Karine; Kamenicky, Peter; Rejnmark, Lars; Linglart, Agnès.
Afiliación
  • Haffner D; Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hannover, Germany. Haffner.Dieter@mh-hannover.de.
  • Emma F; Center for Congenital Kidney Diseases, Center for Rare Diseases, Hannover Medical School, Hannover, Germany. Haffner.Dieter@mh-hannover.de.
  • Eastwood DM; Department of Pediatric Subspecialties, Division of Nephrology, Children's Hospital Bambino Gesù - IRCCS, Rome, Italy.
  • Duplan MB; Department of Orthopaedics, Great Ormond St Hospital for Children, Orthopaedics, London, UK.
  • Bacchetta J; The Catterall Unit Royal National Orthopaedic Hospital NHS Trust, Stanmore, UK.
  • Schnabel D; Dental School, Université Paris Descartes Sorbonne Paris Cité, Montrouge, France.
  • Wicart P; APHP, Department of Odontology, Bretonneau Hospital, Paris, France.
  • Bockenhauer D; APHP, Reference Center for Rare Diseases of Calcium and Phosphate Metabolism, and Filière OSCAR, Paris, France.
  • Santos F; Department of Pediatric Nephrology, Rheumatology and Dermatology, University Children's Hospital, Lyon, France.
  • Levtchenko E; Center for Chronic Sick Children, Pediatric Endocrinology, Charitè, University Medicine, Berlin, Germany.
  • Harvengt P; APHP, Reference Center for Rare Diseases of Calcium and Phosphate Metabolism, and Filière OSCAR, Paris, France.
  • Kirchhoff M; APHP, Department of Pediatric Orthopedic Surgery, Necker - Enfants Malades University Hospital, Paris, France.
  • Di Rocco F; Paris Descartes University, Paris, France.
  • Chaussain C; University College London, Centre for Nephrology and Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Brandi ML; Hospital Universitario Central de Asturias (HUCA), University of Oviedo, Oviedo, Spain.
  • Savendahl L; Department of Pediatric Nephrology and Development and Regeneration, University Hospitals Leuven, University of Leuven, Leuven, Belgium.
  • Briot K; RVRH-XLH, French Patient Association for XLH, Suresnes, France.
  • Kamenicky P; Phosphatdiabetes e.V., German Patient Association for XLH, Lippstadt, Germany.
  • Rejnmark L; Pediatric Neurosurgery, Hôpital Femme Mère Enfant, Centre de Référence Craniosténoses, Université de Lyon, Lyon, France.
  • Linglart A; Dental School, Université Paris Descartes Sorbonne Paris Cité, Montrouge, France.
Nat Rev Nephrol ; 15(7): 435-455, 2019 07.
Article en En | MEDLINE | ID: mdl-31068690
X-linked hypophosphataemia (XLH) is the most common cause of inherited phosphate wasting and is associated with severe complications such as rickets, lower limb deformities, pain, poor mineralization of the teeth and disproportionate short stature in children as well as hyperparathyroidism, osteomalacia, enthesopathies, osteoarthritis and pseudofractures in adults. The characteristics and severity of XLH vary between patients. Because of its rarity, the diagnosis and specific treatment of XLH are frequently delayed, which has a detrimental effect on patient outcomes. In this Evidence-Based Guideline, we recommend that the diagnosis of XLH is based on signs of rickets and/or osteomalacia in association with hypophosphataemia and renal phosphate wasting in the absence of vitamin D or calcium deficiency. Whenever possible, the diagnosis should be confirmed by molecular genetic analysis or measurement of levels of fibroblast growth factor 23 (FGF23) before treatment. Owing to the multisystemic nature of the disease, patients should be seen regularly by multidisciplinary teams organized by a metabolic bone disease expert. In this article, we summarize the current evidence and provide recommendations on features of the disease, including new treatment modalities, to improve knowledge and provide guidance for diagnosis and multidisciplinary care.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Raquitismo Hipofosfatémico Familiar Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline Límite: Humans Idioma: En Revista: Nat Rev Nephrol Asunto de la revista: NEFROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Raquitismo Hipofosfatémico Familiar Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline Límite: Humans Idioma: En Revista: Nat Rev Nephrol Asunto de la revista: NEFROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido