... is properly cited. Abstract X-linked hypophosphataemia (XLH) is a rare genetic disorder that leads to rickets, osteomalacia, and other skeletal abnormalities. Many people with XLH get support from informal caregivers, often family members, to help with their daily living. Although generally rewarding, being...

... Attribution License ( https://creativecommons.org/licenses/by/4.0/ ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract X-linked hypophosphataemia (XLH) is a rare, X-linked dominant condition with a high burden of both...

... of this risk is needed with consideration of alternate iron formulations preferentially in those receiving medications for osteoporosis. If these agents are given simultaneously, increased monitoring of phosphate and calcium levels should be undertaken. Hypophosphataemia Iron infusion Hypocalcaemia...

...Tadayasu Kawaguchi; Yasuji Inamo ABSTRACT We report an 11-year-old girl with systemic lupus erythematosus (SLE) who showed hypophosphataemia (1.7 mg/dl, normal range: 3.9–5.8 mg/dl), a decrease in the tubular maximum reabsorption of phosphate/glomerular filtration rate (TmP/GFR) (0.77 mg/dl...

... kidney injury hypophosphataemia kidney replacement therapy sustained low-efficiency dialysis FIGURE 2: Mean serum phosphate concentration and incidence of hypophosphataemia at the end of each subsequent SLED session. ( A ) Estimated mean values of serum phosphate concentration at the end of each...

... Pediatr 2008 ; 167 : 493 – 9 . 7 Hawley S , Shaw NJ , Delmestri A et al Prevalence and mortality of individuals with X-linked hypophosphataemia: a United Kingdom real world data analysis . J Clin Endocrinol Metab 2020 ; 105 : 1 – 8 . 8 Herrett E , Gallagher AM...

..., hypophosphataemia was defined as a value under the laboratory threshold of 0.78 mmol/L. Asma Alla and Alice Corbel contributed equally to this work. Correspondence to: Raphaël Kormann; E-mail: [email protected] 05 05 2020 11 05 2020 © The Author(s) 2020. Published by Oxford University Press on behalf...

...Pierre-Emmanuel Cailleaux; Seddik Benarbia; Guillaume Allard; Pablo Ureña-Torres; Martine Cohen-Solal dialysis hypophosphataemia osteomalacia periprosthetic fracture A 52-year-old haemodialysis patient was referred in 2015 for mechanical pain in the left hip. His medical history began in 1985...

... (IV) iron can modulate fibroblast growth factor 23 (FGF23) concentrations and cause transient but significant hypophosphataemia. However, it is unknown what other markers might be involved, especially in different patient groups. This study aimed to determine changes in bone and haematinic biomarkers...

... hyperparathyroidism was considered to be the cause of post-transplant hypophosphataemia [ 11 ]; however, it was subsequently observed that hypophosphataemia can persist even after elevated PTH levels have normalized, hence the role of FGF23 was discovered [ 12 , 13 ]. Recent studies suggest that elevated FGF23...

...Gabriela Godaly; Ola Carlsson; Marcus Broman critically ill patients CRRT hypophosphataemia intensive care medicine Electrolyte disorders frequently develop in critically ill patients treated at the intensive care unit (ICU) [ 1 ]. The onset of acute kidney injury (AKI), which occurs in up...

... for the potential occurrence of Fanconi syndrome. Measurement of the urinary albumin:total protein ratio is a suggested screening tool for tubular proteinuria in Fanconi syndrome. fumarates hypophosphataemia osteomalacia proteinuria proximal tubular dysfunction Fumaric acid esters (FAEs) are small molecules...

.../chorus/standard_publication_model ) Hypophosphataemia usually presents in childhood. This report describes, however, a case of hypophosphataemic rickets diagnosed in an adult female who presented complaining of generalized dental hypersensitivity. Radiographic examination revealed a discrete, generalized...

... kidney recipient outcomes. fibroblast growth factor 23 hyperparathyroidism hypophosphataemia kidney transplantation post-transplant bone disease Mineral and bone disorders are common in patients who have undergone kidney transplantation [ 1 ]. These conditions are caused, to a large extent, by pre...

...Rodrigo Azevedo de Oliveira; Igor Denizarde Bacelar Marques; Antonio Carlos Seguro; Lúcia Andrade In the case described here, the patient developed various hypoelectrolyte disorders (hypokalaemia, hypophosphataemia and hypomagnesaemia). This occurred even in the presence of AKI. Early diagnosis...

...), hypomagnesaemia in 17% (8/47), hypocalaemia in 6% (2/34) and hypophosphataemia in 6% (2/31) of the patients. Overall, 21% (10/48) had one or more electrolyte abnormalities at baseline. Following autologous HSCT, hypokalaemia occurred in 81% (39/48), hypomagnesaemia in 67% (32/48), hypocalcaemia in 49% (17/35...

... on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: [email protected] 2007 high fibroblast growth factor (FGF23) hypophosphataemia phosphaturia dentin matrix protein 1 (DMP1) There are several hypophosphataemic disorders attributed to the phosphaturic effect...

... or a significant change in renal function. adefovir dipivoxil hepatitis B HIV infection hypophosphataemia nephrotoxicity renal tolerance tubulopathy Lamivudine (LAM)-resistant hepatitis B virus (HBV) is found in ∼15–32% of infected patients, with or without HIV-1 infection, after 1 year of LAM therapy [ 1...

... at 8 and 12 weeks after transplantation as compared with groups 2 and 3. At 20 weeks after transplantation, patients with rapamycin‐based immunosuppression (groups 1A and 1B) continued to exhibit hypophosphataemia and impaired renal phosphate handling. Group 1B had the lowest TmP/ GFR compared with all...

..., Harvey JM, Vale JA. Hypophosphataemia and phosphaturia in paracetamol poisoning. Lancet 1989 ; 2 : 608 –609 7 Mitchell JR, McMurtry RJ, Statham CN, Nelson SD. Molecular basis for several drug-induced nephropathies. Am J Med 1977 ; 62 : 518 –526 8 Eckardt K-U. Renal...