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- W3136178170 abstract "Alport syndrome is a rare inheritable renal disease characterized by renal, cochlear, and ocular involvement. Patients commonly require renal replacement therapy in the second or third decade of life. Renal transplantation in pediatric patients has become a routinely successful procedure, with 1- and 5-year patient survival rates of 98%, the range takes into account the differences between living and deceased donors. These good outcomes represent the cumulative effect of improvements in pre- and post-transplant patient care, operative techniques, immunosuppression, and infection prophylaxis, diagnosis, and treatment. We report the case of a male child with Alport syndrome who underwent preemptive live renal transplant and his mother was the donor." @default.
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- W3136178170 date "2017-01-01" @default.
- W3136178170 modified "2023-09-26" @default.
- W3136178170 title "Renal transplant in a child with Alport syndrome" @default.
- W3136178170 doi "https://doi.org/10.4103/ijot.ijot_22_17" @default.
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