Autosomal Dominant Hypophosphatemic Rickets: A Case Report and Review of the Literature

Autosomal dominant hypophosphatemic rickets (ADHR) is an extremely rare form of genetic rickets caused by mutations in the fibroblast growth factor 23 gene. ADHR is characterized by hypophosphatemia secondary to isolated renal phosphate wasting. Only a few cases of ADHR have been reported in the lit...

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Detalles Bibliográficos
Autores principales: Mameli, Chiara, Sangiorgio, Arianna, Colombo, Valeria, Gambino, Mirko, Spaccini, Luigina, Cattaneo, Elisa, Zuccotti, Gian Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392413/
https://www.ncbi.nlm.nih.gov/pubmed/34444516
http://dx.doi.org/10.3390/ijerph18168771

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392413/
https://www.ncbi.nlm.nih.gov/pubmed/34444516
http://dx.doi.org/10.3390/ijerph18168771

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