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Contribution of imaging to the diagnosis and follow up of X-linked hypophosphatemia.
Adamsbaum, Catherine; Laredo, Jean-Denis; Briot, Karine; Linglart, Agnès.
Afiliação
  • Adamsbaum C; Université de Paris Saclay, AP-HP, Département de Radiologie Pédiatrique, Hôpital Bicêtre Paris Saclay, 78 rue du Général Leclerc, 94275 Le Kremlin-Bicêtre, France. Electronic address: Catherine.adamsbaum@aphp.fr.
  • Laredo JD; AP-HP, Department of Radiology, Lariboisière Hospital, Paris, France.
  • Briot K; AP-HP, Department of Rheumatology, Cochin Hospital, Paris, France.
  • Linglart A; Université de Paris Saclay, AP-HP, Centre de Référence des maladies rares du métabolisme du Calcium et du Phosphate, filière OSCAR, service d'endocrinologie et diabète de l'enfant, hôpital Bicêtre Paris Saclay, Le Kremlin Bicêtre, France.
Arch Pediatr ; 28(7): 594-598, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34583869
X-linked hypophosphatemia (XLH) is the most common form of inheritable rickets. The disease is caused principally by PHEX mutations leading to increased concentrations of circulating intact FGF23, hence renal phosphate wasting, hypophosphatemia, and decreased circulating levels of 1,25(OH)2 vitamin D. The chronic hypophosphatemia leads to rickets and osteomalacia through a combination of mechanisms, including a lack of endochondral ossification and impaired mineralization. Imaging has a major role in determining the diagnosis of rickets and its cause, detecting complications as early as possible, and helping in treatment monitoring.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diagnóstico por Imagem / Raquitismo Hipofosfatêmico Familiar Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Arch Pediatr Ano de publicação: 2021 Tipo de documento: Article País de publicação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diagnóstico por Imagem / Raquitismo Hipofosfatêmico Familiar Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Arch Pediatr Ano de publicação: 2021 Tipo de documento: Article País de publicação: França