Results 11 to 20 of about 29,515 (111)

Bilateral atraumatic neck of femur fractures secondary to tenofovir-induced fanconi syndrome

open access: yesJournal of Orthopaedic Reports, 2023
Background: Tenofovir is an effective drug in the treatment of chronic hepatitis B. However, it has been associated with adverse complication of Fanconi syndrome due to proximal renal tubule dysfunction.
Vikaesh Moorthy, Kelvin Guoping Tan
doaj   +1 more source

Nephrolithiasis and Osteomalacia associated with adefovir-induced Fanconi syndrome in a patient with hepatitis B

open access: yesBMC Nephrology, 2017
Background An increasing number of case reports suggest that acquired renal Fanconi syndrome may be associated with prolonged use of adefovir against hepatitis B virus.
Jueying Lin, Yufeng Zhuo, Dongdong Zhang
doaj   +1 more source

Oral and Dental Manifestations of Fanconi Anemia

open access: yesGalician Medical Journal, 2021
Fanconi anemia is a rare disease, which is characterized by decreased production of all blood cell types. Fanconi anemia is the most common inherited form of aplastic anemia.
Vesna Ambarkova
doaj   +1 more source

Renal Sarcoidosis Presenting as Fanconi Syndrome

open access: yesAnnals of Internal Medicine: Clinical Cases, 2023
Fanconi syndrome is an extremely rare complication of renal sarcoidosis. We describe a case of biopsy-proven granulomatous interstitial nephritis secondary to sarcoidosis with the rare presenting feature of Fanconi syndrome.
Suma Prakash   +3 more
doaj   +1 more source

Transient acquired Fanconi syndrome with unusual and rare aetiologies: A case study of two dogs

open access: yesVeterinární Medicína, 2020
The acquired form of Fanconi syndrome is seldom identified in dogs; those cases that have been reported have been secondary to hepatic copper toxicosis, primary hypoparathyroidism, ingestion of chicken jerky treats, exposure to ethylene glycol, or ...
Ju-Yong Park   +3 more
doaj   +1 more source

HNF4A-related Fanconi syndrome in a Chinese patient: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2018
Background The p.R63W mutation in hepatocyte nuclear factor-4 alpha (HNF4A) leads to a heterogeneous group of disorders with various clinical presentations.
Jiaojiao Liu   +3 more
doaj   +1 more source

Invasive Pneumococcal Disease Associated with Fanconi-Like Syndrome

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2019
Acquired causes of Fanconi syndrome in adults are usually due to drugs, toxins or paraproteinaemias. Infectious causes are rarely described. We report a case of invasive pneumococcal disease in a patient who developed a Fanconi-like syndrome during the ...
Jade Xiao Jue Soh   +2 more
doaj   +1 more source

Proximal renal tubular acidosis with and without Fanconi syndrome

open access: yesKidney Research and Clinical Practice, 2019
Proximal renal tubular acidosis (RTA) is caused by a defect in bicarbonate (HCO3−) reabsorption in the kidney proximal convoluted tubule. It usually manifests as normal anion-gap metabolic acidosis due to HCO3− wastage.
Ibrahim Kashoor, Daniel Batlle
doaj   +1 more source

Anesthesia for a patient with Fanconi anemia for developmental dislocation of the hip: a case report

open access: yesBrazilian Journal of Anesthesiology, 2014
Fanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with congenital and hematological abnormalities. Literature regarding the anesthetic management in these patients is limited.
Zafer Dogan   +4 more
doaj   +3 more sources

A Fanconi-Bickel syndrome patient with a novel mutation and accompanying situs inversus totalis

open access: yesThe Turkish Journal of Pediatrics, 2017
Fanconi-Bickel syndrome is a rare autosomal recessive disorder of carbohydrate metabolism, caused by mutations in the SLC2A2 gene, that codes for the glucose transporter protein 2 (GLUT2).
Tuğba Taştemel-Öztürk   +3 more
doaj   +1 more source

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