Results 11 to 20 of about 2,262,684 (231)

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

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
doaj   +2 more sources

Two Cases of Chronic Tubular Necrosis Presenting as Fanconi Syndrome Induced by Red Yeast Rice Choleste-Help [PDF]

Diagnostics
Background and Clinical Significance: Although dietary supplements have often been deemed safe, some have been linked to drug-induced nephropathy due to their diverse ingredients.
Kanako Mita, Shunsuke Takahashi, Satoshi Yanagida, Akihiro Aoyama, Takayuki Shiraishi, Takayuki Hamada, Yumiko Nakamura, Mariko Sato, Kento Hirose, Ryo Yamamoto, Yuya Shioda, Kaori Takayanagi, Izumi Nagayama, Yuko Ono, Hajime Hasegawa, Akito Maeshima   +15 more
doaj   +2 more sources

A case of acute kidney injury and Fanconi syndrome while taking multiple supplements, including Red Yeast Rice Cholesterol Help^®. [PDF]

CEN Case Rep
A 62-year-old man visited his primary care physician with the complaints of loss of appetite and fatigue. He was admitted to our hospital based on a diagnosis of acute kidney injury, Fanconi syndrome as indicated by hypokalemia, hypouricemia ...
Oda K, Murata T, Tanaka F, Oda H, Tsujimoto K, Fukumori A, Yamawaki M, Saiki R, Suzuki Y, Katayama K, Dohi K.   +10 more
europepmc   +2 more sources

Fanconi syndrome with acute proximal tubular injury induced by a dietary supplement containing beni-koji: a case series report [PDF]

BMC Nephrology
Background Fanconi syndrome is a disorder of the proximal tubule that leads to malabsorption of various electrolytes and substances and is a common consequence of drug-induced nephrotoxicity.
Masato Habuka, Michihiro Hosojima, Yusuke Yata, Kenshiro Kurumada, Moeri Yamagiwa, Masataka Yonezawa, Masanori Sudo, Hideyuki Kabasawa, Asa Ogawa, Hitomi Hama, Yumi Ito, Naofumi Imai, Suguru Yamamoto, Akihiko Saito, Shin Goto   +14 more
doaj   +2 more sources

Acquired Fanconi Syndrome from Tenofovir Treatment in a Patient with Hepatitis B [PDF]

Case Reports in Hepatology, 2023
Fanconi syndrome is a rare disease of generalized proximal tubule dysfunction which can be acquired secondary to certain medications, including tenofovir, a commonly used hepatitis B treatment.
Shirley X. Jiang, John Duncan, Hin Hin Ko   +2 more
doaj   +2 more sources

Fanconi–Bickel syndrome in a Ugandan child – diagnostic challenges in resource-limited settings: a case report [PDF]

Journal of Medical Case Reports, 2020
Background Fanconi–Bickel syndrome is an autosomal recessive disorder of glucose metabolism. It is an extremely rare disorder. Most cases have been reported in consanguineous communities.
Thereza Piloya, Hawa Ssematala, Lydia Paparu Dramani, Oliva Nalikka, Miriam Baluka, Victor Musiime   +5 more
doaj   +2 more sources

The recurrent p.Glu3Lys variant in EHHADH is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalities [PDF]

Molecular Genetics and Metabolism Reports
Background: The recurrent pathogenic variant c.7G>A p.Glu3Lys in the EHHADH gene is responsible for an autosomal dominant form of Fanconi renotubular syndrome.
P. Rollier, A. Cospain, M. Barth, V. Milon, N. Gueguen, C. Homedan, V. Desquiret, C. Bris, E. Colin, L. Damaj, A. Ryckewaert, P. Reynier, S. Odent, P. Amati-Bonneau, V. Procaccio, D. Bonneau, A. Ziegler   +16 more
doaj   +2 more sources

Osteomalacia, renal Fanconi syndrome, and bone tumor

Journal of International Medical Research, 2018
We herein report two cases of Fanconi syndrome with refractory hypophosphatemic osteomalacia that was difficult to correct by phosphorus replacement therapy.
Manting Gou, Zhongshu Ma
doaj   +2 more sources

Renal Fanconi Syndrome Is Caused by a Mistargeting-Based Mitochondriopathy

Cell Reports, 2016
Summary: We recently reported an autosomal dominant form of renal Fanconi syndrome caused by a missense mutation in the third codon of the peroxisomal protein EHHADH.
Nadine Assmann, Katja Dettmer, Johann M.B. Simbuerger, Carsten Broeker, Nadine Nuernberger, Kathrin Renner, Holly Courtneidge, Enriko D. Klootwijk, Axel Duerkop, Andrew Hall, Robert Kleta, Peter J. Oefner, Markus Reichold, Joerg Reinders   +13 more
doaj   +2 more sources

Lysinuric protein intolerance exhibiting renal tubular acidosis/Fanconi syndrome in a Japanese woman [PDF]

JIMD Reports, 2023
Lysinuric protein intolerance (LPI), caused by pathogenic variants of SLC7A7, is characterized by protein aversion, failure to thrive, hyperammonemia, and hepatomegaly.
Hiroaki Hanafusa, Katsuya Nakamura, Yuji Kamijo, Masashi Kitahara, Takashi Ehara, Tsuneaki Yoshinaga, Kaoru Aoki, Nagaaki Katoh, Tomomi Yamaguchi, Tomoki Kosho, Yoshiki Sekijima   +10 more
doaj   +2 more sources