Intravenous iron-induced hypophosphatemia and kidney stone disease

Autor: Marlene Panzer, Eva Meindl, Benedikt Schaefer, Sonja Wagner, Bernhard Glodny, Gert Mayer, Andreas Pircher, Christoph Schwarz, Felix Beckmann, Clivia Hejny, Bastian Joachim-Mrosko, Juergen Konzett, Herbert Tilg, Isabel Heidegger, Myles Wolf, Ralf Weiskirchen, Heinz Zoller

Publikováno v: Bone Reports, Vol 21, Iss , Pp 101759- (2024)

Patients with Crohn's disease are at increased risk for symptomatic nephrolithiasis. Stones in these patients are most commonly composed of calcium oxalate monohydrate or mixed calcium-oxalate and calcium-phosphate. Precipitation of both minerals dep

Externí odkaz: https://doaj.org/article/55260aad10e4454a9c237111d053e33b

Hypophosphatemic rickets: pathogenesis, diagnosis and treatment

Autor: Kristina S. Kulikova, Anatoly N. Tiulpakov

Publikováno v: Ожирение и метаболизм, Vol 15, Iss 2, Pp 46-50 (2018)

Hypophosphatemic rickets (HR) - a group of diseases characterized by the development of ricketic changes in bone tissue due to increased excretion of phosphorus from the body. This form of rickets is the most common among variants of genetically dete

Externí odkaz: https://doaj.org/article/4f7f00f2b1ef41fa9e47521923157bb4

Unusual presentation of a five‐month‐old boy with NaPi2a homozygous mutation without hyperphosphaturia: Case report and review of the literature

Autor: Machiel van den Akker, Asaly Ayman, An Bael, Renata Yakubov, Adi Kremer

Publikováno v: Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Clinical Case Reports

Deletions of the NaPi2a gene and mutations in the SLC34A gene should be considered in patients with atypical presentation, without phosphaturia, with mild hypo to normal phosphatemia, and nephrocalcinosis.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8cc0f89d47de27e1231137047cbd384
https://doaj.org/article/2d6fb48963c64e3cbb907431d48355a4

Renal Phosphate Wasting Due to Tumor-Induced (Oncogenic) Osteomalacia

Autor: Ragarupa Kotala, James Kamau, Richard Snyder, Emily B Ernst, Eluwana A Amaratunga

Publikováno v: Cureus

Osteomalacia is a widely prevalent bone disorder that is caused by an imbalance in body calcium and phosphate. Tumor-induced osteomalacia (TIO) is a rare form of osteomalacia that is associated with mesenchymal tumors. It is caused by overproduction

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01017f67ba1c8b745e9d1a5a4f24c78d
https://doi.org/10.7759/cureus.15507

A physiological approach to recurrent nephrolithiasis and its genetic determinants

Autor: Fonseca, Nuno Moreira, Livrozet, Marine, Varga-Poussou, Rosa, Letavernier, Emmanuel, Frochot, Vincent, Daudon, Michel, Haymann, Jean-Philippe

Publikováno v: Portuguese Journal of Nephrology & Hypertension v.34 n.1 2020
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Portuguese Journal of Nephrology & Hypertension, Volume: 34, Issue: 1, Pages: 61-63, Published: MAR 2020

We report a case of a 63-year-old patient with recurrent nephrolithiasis for over 40 years and a significant family history of nephrolithiasis. The patient underwent full investigation at our department. He presented hypercalcemia, hypophosphatemia a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bc8f1cf3470713bb8a86b3d18f43a69d
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-01692020000100012