A rare case of concomitant hypophosphatemic osteomalacia and neurofibromatosis type 1

INTRODUCTION: Neurofibromatosis type 1 is a rare genetic disorder with an increased susceptibility to develop skeletal abnormalities. However, the association of hypophosphatemic osteomalacia and neurofibromatosis type 1 is extremely rare. Herein, we report a case of hypophosphatemic osteomalacia in...

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Detalles Bibliográficos
Autores principales: Şehit Kara, Canan, Hacıoğlu, Ayşa, Karaca, Züleyha, Ünlühızarcı, Kürşad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Bone & Calcium
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653172/
http://dx.doi.org/10.1210/jcemcr/luac014.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653172/
http://dx.doi.org/10.1210/jcemcr/luac014.011

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