Tubulopathy - Open Access .click

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Repurposing SGLT2 inhibitors:Treatment of renal proximal tubulopathy in Fanconi-Bickel syndrome with empagliflozin [PDF]

Renal proximal tubulopathy in Fanconi-Bickel syndrome is caused by impaired basolateral glucose transport via GLUT2 and consequently, intracellular accumulation of glucose and glycogen.
Besouw, Martine T.P. +13 more
core +1 more source

sj-docx-5-tpx-10.1177_01926233231191128 – Supplemental material for Comparative Analysis of Hypertensive Tubulopathy in Animal Models of Hypertension and Its Relevance to Human Pathology

, 2023
Supplemental material, sj-docx-5-tpx-10.1177_01926233231191128 for Comparative Analysis of Hypertensive Tubulopathy in Animal Models of Hypertension and Its Relevance to Human Pathology by Alex A. Gutsol, Taben M.
Rania Nasrallah (12102213) +10 more
core +1 more source

HYPOPHOSPHATEMIC RICKETS

Педиатрическая фармакология, 2013
The article describes modern views on etiology and pathogenesis of various variants of hypophosphatemic rickets and main approaches to diagnostics and treatment of this disease; it also presents a range of clinical cases from the authors’ practice.
N. N. Kartamysheva +9 more
doaj +1 more source

sj-docx-6-tpx-10.1177_01926233231191128 – Supplemental material for Comparative Analysis of Hypertensive Tubulopathy in Animal Models of Hypertension and Its Relevance to Human Pathology

, 2023
Supplemental material, sj-docx-6-tpx-10.1177_01926233231191128 for Comparative Analysis of Hypertensive Tubulopathy in Animal Models of Hypertension and Its Relevance to Human Pathology by Alex A. Gutsol, Taben M.
Rania Nasrallah (12102213) +10 more
core +1 more source

Reduced Expression of Magnesium Transport Proteins in the Distal Convoluted Tubule of Clcnkb‐Deficient Mice May Explain Urinary Magnesium Wasting in Classical Bartter Syndrome

Acta Physiologica, Volume 242, Issue 9, September 2026.
ABSTRACT Aim The kidney thick ascending limb (TAL) plays a key role in the transport of sodium, chloride, potassium, calcium, and magnesium. Bartter syndrome is a hypokalemic, salt‐losing tubulopathy caused by impaired TAL function. Pathogenic variants in SLC12A1 or KCNJ1 cause antenatal Bartter syndrome, and variants in CLCNKB result in classical ...
Marleen L. A. Kortenoeven +12 more
wiley +1 more source

Chemotherapy-induced tubulopathy: a case report series

Frontiers in Nephrology
Acquired tubulopathies are frequently underdiagnosed. They can be characterized by the renal loss of specific electrolytes or organic solutes, suggesting the location of dysfunction.
Mario Alamilla-Sanchez +6 more
doaj +1 more source

Urine electrolytes guide treatment of Gitelman syndrome and recurrent syncope—A case report

Physiological Reports, Volume 14, Issue 18, September 2026.
Abstract Syncope is a common reason for inpatient admission. Few case studies describe an association between syncope and Gitelman syndrome (GS). Herein, we present a case of a woman with hypokalemia and recurrent syncope which eventually led to a diagnosis of GS. A physiologic approach to urine electrolyte interpretation informed clinical decisions to
Saloni Agrawal +3 more
wiley +1 more source

Concurrent light chain amyloidosis and proximal tubulopathy: Insights into different aggregation behavior—A case report

, 2022
Due to differences in the protein folding mechanisms, it is exceedingly rare for amyloid light chain (AL) amyloidosis and monoclonal gammopathy of renal significance (MGRS) to coexist.
Zoller, Julian +27 more
core +1 more source

Transient Renal Tubulopathy: A Case Report

Renal Failure, 2008
A five-year-old boy was evaluated for fever, abdominal pain, vomiting, and diarrhea lasting two days. Chest radiograph revealed a left bronchopneumonia. Metabolic work-up demonstrated phosphaturia, glucosuria, calciuria, proteinuria, profound hypophosphatemia, hypouricemia, borderline hypomagnesemia, and normoglycemia.
Shira, Shacham +3 more
openaire +2 more sources

Clinical Characteristics, Symptoms, and Long-Term Outcomes in Gitelman Syndrome

Kidney International Reports
Introduction: Gitelman syndrome (GS) is a rare inherited salt-losing tubulopathy with limited clinical data. Methods: Surveys were conducted with GS physicians in Europe and patients with GS in the Netherlands to compare findings with the general ...
Michiel L.A.J. Wieërs +65 more
doaj +1 more source

children
gitelman syndrome
hypokalemia

adrenal glands
aldosterone
diagnostics

multiple myeloma