Cargando…
Outcomes of orthopedic surgery in a cohort of 49 patients with X-linked hypophosphatemic rickets (XLHR)
BACKGROUND: X-linked hypophosphatemic rickets (XLHR) is due to mutations in PHEX leading to unregulated production of FGF23 and hypophosphatemia. XLHR is characterized by leg bowing of variable severity. Phosphate supplements and oral vitamin analogs, partially or, in some cases, fully restore the l...
Autores principales: | Gizard, A, Rothenbuhler, A, Pejin, Z, Finidori, G, Glorion, C, de Billy, B, Linglart, A, Wicart, P |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633063/ https://www.ncbi.nlm.nih.gov/pubmed/28954742 http://dx.doi.org/10.1530/EC-17-0154 |
Ejemplares similares
-
High Incidence of Cranial Synostosis and Chiari I Malformation in Children With X‐Linked Hypophosphatemic Rickets (XLHR)
por: Rothenbuhler, Anya, et al.
Publicado: (2018) -
Therapeutic management of hypophosphatemic rickets from infancy to adulthood
por: Linglart, Agnès, et al.
Publicado: (2014) -
Prospective Analysis of Muscle Adiposity in Children With X-linked Hypophosphatemic Rickets vs Control Children
por: Nguyen-Khac, Virginie, et al.
Publicado: (2022) -
Papilledema in the Setting of X-Linked Hypophosphatemic Rickets with Craniosynostosis
por: Glass, Lora R. Dagi, et al.
Publicado: (2011) -
X-linked hypophosphatemic rickets: a new mutation
por: Maio, Patrícia, et al.
Publicado: (2020)