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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...

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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

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