Literature DB >> 30454741

Fanconi Syndrome.

John W Foreman1.   

Abstract

Fanconi syndrome, also known as the DeToni, Debré, Fanconi syndrome is a global dysfunction of the proximal tubule characterized by glucosuria, phosphaturia, generalized aminoaciduria, and type II renal tubular acidosis. Often there is hypokalemia, sodium wasting, and dehydration. In children, it typically is caused by inborn errors of metabolism, principally cystinosis. In adults, it is mainly caused by medications, exogenous toxins, and heavy metals. Treatment consists of treating the underlying cause and replacing the lost electrolytes and volume.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cystinosis; Dent disease; Fanconi syndrome; Lowe syndrome; Proximal tubule

Mesh:

Year:  2019        PMID: 30454741     DOI: 10.1016/j.pcl.2018.09.002

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN: 0031-3955            Impact factor:   3.278


  17 in total

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4.  Renal Deletion of LRRC8/VRAC Channels Induces Proximal Tubulopathy.

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6.  Clinicopathological characteristics and long-term prognosis of monoclonal immunoglobulin light chain associated Fanconi syndrome.

Authors:  Zhixin Chen; Jiaying Li; Xiaoxiao Shi; Ying Wang; Peng Xia; Wei Ye; Wenling Ye; Yan Qin; Hang Li; Mingxi Li; Xuemei Li; Yubing Wen; Limeng Chen
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7.  Invasive Pneumococcal Disease Associated with Fanconi-Like Syndrome.

Authors:  Jade Xiao Jue Soh; Raymond Kai Heng Goh; Shuwei Zheng
Journal:  Eur J Case Rep Intern Med       Date:  2019-09-27

8.  Clinical manifestation and genetic findings in three boys with low molecular Weight Proteinuria - three case reports for exploring Dent Disease and Fanconi syndrome.

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Journal:  BMC Nephrol       Date:  2021-01-11       Impact factor: 2.388

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10.  Non-diabetic glycosuria as a diagnostic clue for acute tubulointerstitial nephritis in patients with azotemia.

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