dent's disease
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2020 ◽  
Vol 9 (4) ◽  
pp. 380-384
Author(s):  
Shinichi Makino ◽  
Maulana A. Empitu ◽  
Toshimasa Naito ◽  
Masayoshi Ishii ◽  
Hanae Wakabayashi ◽  
...  

2019 ◽  
Vol 44 (5) ◽  
pp. 1306-1312 ◽  
Author(s):  
Giovanni Gambaro ◽  
Alessandro Naticchia ◽  
Pietro Manuel Ferraro ◽  
Gionata Spagnoletti ◽  
Jacopo Romagnoli ◽  
...  

Introduction: Dent’s disease is a rare X-linked recessive disorder that manifests in childhood or early adulthood and can lead to end-stage renal disease (ESRD). It occurs in males, who are hemizygous. In patients who develop ESRD, a deceased donor kidney transplant cures the disease. Females are obligate carriers of the mutated gene, and some show a mild Dent’s disease phenotype. There may be reason for concern when considering a female obligate carrier (i.e., the mother) for kidney donation because of the risk of kidney function deterioration. Case Presentation: We describe the first successful kidney transplantation involving a patient with type 1 Dent’s disease and ESRD given a kidney by an obligate carrier of the gene mutation, his mother. Conclusions: After careful assessment of the female obligate carriers, intrafamilial kidney donation in Dent’s disease type 1 is feasible. No deteriorating renal function in the donor was observed.


Gene ◽  
2018 ◽  
Vol 649 ◽  
pp. 23-26 ◽  
Author(s):  
Roman Günthner ◽  
Matias Wagner ◽  
Tobias Thurm ◽  
Sabine Ponsel ◽  
Julia Höfele ◽  
...  

2018 ◽  
Vol 22 (2) ◽  
pp. 74-80
Author(s):  
L. S. Prikhodina ◽  
S. V. Papizh ◽  
Z. R. Bashirova ◽  
M. Ludwig

2017 ◽  
Vol 36 (12) ◽  
pp. 1151-1158 ◽  
Author(s):  
Ya Zhang ◽  
Xiaoyan Fang ◽  
Hong Xu ◽  
Qian Shen

2017 ◽  
Vol 11 (4) ◽  
pp. 459-461 ◽  
Author(s):  
Anne Sophie Fischer ◽  
Niels Marcussen ◽  
Maria Rasmussen ◽  
Else Randers

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