Cargando…
Young XLH Patients-Reported Experience with a Supportive Care Program
PURPOSE: X-linked hypophosphatemia (XLH) is a rare, chronic, genetic condition characterized by renal phosphate wasting and abnormal bone and teeth mineralization. It represents a challenging and multifaceted disease that causes wide-ranging impacts on patients’ lives. In this context, a scientific...
Autores principales: | Rothenbuhler, Anya, Gueorguieva, Iva, Lichtenberger-Geslin, Lydia, Audrain, Christelle, Soskin, Sylvie, Bensignor, Candace, Rossignol, Sylvie, Bertholet-Thomas, Aurélia, Naudeau, Lorelei, Bacchetta, Justine, Linglart, Agnès |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10263015/ https://www.ncbi.nlm.nih.gov/pubmed/37325587 http://dx.doi.org/10.2147/PPA.S391025 |
Ejemplares similares
-
XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH)
por: Seefried, Lothar, et al.
Publicado: (2023) -
Growth pattern in children with X-linked hypophosphatemia treated with burosumab and growth hormone
por: Ertl, Diana-Alexandra, et al.
Publicado: (2022) -
A randomized pilot trial of growth hormone with anastrozole versus growth hormone alone, starting at the very end of puberty in adolescents with idiopathic short stature
por: Rothenbuhler, Anya, et al.
Publicado: (2015) -
Erratum to: A randomized pilot trial of growth hormone with anastrozole versus growth hormone alone, starting at the very end of puberty in adolescents with idiopathic short stature
por: Rothenbuhler, Anya, et al.
Publicado: (2017) -
High Incidence of Cranial Synostosis and Chiari I Malformation in Children With X‐Linked Hypophosphatemic Rickets (XLHR)
por: Rothenbuhler, Anya, et al.
Publicado: (2018)