Neurofibromatosis type 1 associated with hypophosphatemic osteomalacia due to hypersecretion of fibroblast growth factor 23: a case report

BACKGROUND: Neurofibromatosis type 1 is characterized by multiple café au lait spots and cutaneous and plexiform neurofibromas, and is one of the most common autosomal dominant hereditary disorders caused by mutations of the neurofibromatosis type 1 tumor suppressor gene. Osteomalacia in neurofibrom...

Descripción completa

Detalles Bibliográficos
Autores principales: Obo, Takahiko, Koriyama, Nobuyuki, Tokito, Akinori, Ogiso, Kazuma, Nishio, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210688/
https://www.ncbi.nlm.nih.gov/pubmed/32384911
http://dx.doi.org/10.1186/s13256-020-02381-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210688/
https://www.ncbi.nlm.nih.gov/pubmed/32384911
http://dx.doi.org/10.1186/s13256-020-02381-1

Ejemplares similares