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Renal Sarcoidosis Presenting as Fanconi Syndrome [PDF]
Annals 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
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Invasive Pneumococcal Disease Associated with Fanconi-Like Syndrome [PDF]
European 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
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BMC 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
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A Fanconi-Bickel syndrome patient with a novel mutation and accompanying situs inversus totalis
The 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
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HNF4A-related Fanconi syndrome in a Chinese patient: a case report and review of the literature
Journal 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
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Oral and Dental Manifestations of Fanconi Anemia
Galician 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
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Fanconi or not Fanconi? Lowe Syndrome Revisited [PDF]
Clinical Journal of the American Society of Nephrology, 2008 Renal Fanconi syndromes are both clinically challenging and physiologically fascinating. The diagnosis requires a certain index of suspicion to correctly identify the clinical symptomatology and pursue the appropriate laboratory evaluations. With regard to the pathophysiology, the renal proximal tubule is the site of action.
openaire +2 more sources
Transient acquired Fanconi syndrome with unusual and rare aetiologies: A case study of two dogs
Veterinární 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
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Proximal renal tubular acidosis with and without Fanconi syndrome
Kidney 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
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Anesthesia for a patient with Fanconi anemia for developmental dislocation of the hip: a case report
Brazilian 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
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