High Incidence of Cranial Synostosis and Chiari I Malformation in Children With X‐Linked Hypophosphatemic Rickets (XLHR)

X‐linked hypophosphatemic rickets (XLHR) represents the most common form of genetic hypophosphatemia and causes rickets and osteomalacia in children because of increased FGF23 secretion and renal phosphate wasting. Even though cranial vault and craniovertebral anomalies of potential neurosurgical in...

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Detalles Bibliográficos
Autores principales: Rothenbuhler, Anya, Fadel, Nathalie, Debza, Yahya, Bacchetta, Justine, Diallo, Mamadou Tidiane, Adamsbaum, Catherine, Linglart, Agnès, Di Rocco, Federico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816089/
https://www.ncbi.nlm.nih.gov/pubmed/30352126
http://dx.doi.org/10.1002/jbmr.3614

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816089/
https://www.ncbi.nlm.nih.gov/pubmed/30352126
http://dx.doi.org/10.1002/jbmr.3614

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