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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...
Autores principales: | Rothenbuhler, Anya, Fadel, Nathalie, Debza, Yahya, Bacchetta, Justine, Diallo, Mamadou Tidiane, Adamsbaum, Catherine, Linglart, Agnès, Di Rocco, Federico |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
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 |
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