Hypophosphatemic osteomalacia in neurofibromatosis 1 associated with intracranial gliomas and congenital renal agenesis: A rare case report and review of the literature

INTRODUCTION: Neurofibromatosis Type 1 (Nf1), also termed von Recklinghausen disease, is a rare autosomal dominant genetic disorder accompanied by several osseous and skeletal manifestations. In NF, hypophosphatemia linked to secondary hyperparathyroidism due to Vitamin D deficiency and low calcium...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaspiris, Angelos, Vasiliadis, Elias, Melissaridou, Dimitra, Iliopoulos, Ilias D, Papagelopoulos, Panayiotis J, Savvidou, Olga D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499154/
https://www.ncbi.nlm.nih.gov/pubmed/36199714
http://dx.doi.org/10.13107/jocr.2022.v12.i02.2650

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499154/
https://www.ncbi.nlm.nih.gov/pubmed/36199714
http://dx.doi.org/10.13107/jocr.2022.v12.i02.2650

Ejemplares similares