Rare cause of pathological fracture in adults as hypophosphatemic rickets

Autor:	Gowtham S. Gowda, K R Divya Sharma, J M Jeetendra Kumar, T R Mamatha
Rok vydání:	2019
Předmět:	Fibroblast growth factor 23 medicine.medical_specialty business.industry Rickets Disease medicine.disease Excretion Hypophosphatemic Rickets Endocrinology Internal medicine medicine Vitamin D and neurology Complication business Pathological
Zdroj:	International Journal of Advances in Medicine. 6:1681
ISSN:	2349-3933 2349-3925
Popis:	Hypophosphatemic rickets is a disorder of defective bone minerlization due to defect in renal phosphate handling process. It is characterised by increased phosphate excretion accompanied by increased phosphatonins like fibroblast growth factor 23. It can be hereditary form of X linked, autosomal dominant, autosomal recessive type of hypophosphatemic rickets. It is associated with low serum phosphorus, normal serum calcium, inappropriately low to normal vitamin D level. Correct identification of these disorders is important for determining therapy. Early diagnosis and management prevent subsequent complication of the disease.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::fac97975f54e277c3488387ffe7266e4 https://doi.org/10.18203/2349-3933.ijam20194242 Zobrazit plný text záznamu