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Information Journal Paper

Title

DELAYED DIAGNOSIS OF ALPORT SYNDROME WITHOUT HEMATURIA (CASE REPORT)

Pages

  250-251

Abstract

 ALPORT SYNDROME is a progressive hereditary disease caused by mutations in the genes encoding type IV collagen. Persistent microscopic HEMATURIA is the hallmark of ALPORT SYNDROME, occurring in almost all boys according to previous reports. We report the case of a 20-year-old man presented with proteinuria but no HEMATURIA that was initially misdiagnosed with refractory nephrotic syndrome and was eventually diagnosed with ALPORT SYNDROME following kidney and skin biopsy. During the followup period, he experienced a rapid progression to end-stage renal disease. Timely diagnosis of ALPORT SYNDROME is important, because patients may benefit from early intervention and avoid suffering from unnecessary nephrotoxic drug use.

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    • Cite

    APA: Copy

    YIN YIN, CHEN, YOU MING, PENG, & YU MEI, LIANG. (2014). DELAYED DIAGNOSIS OF ALPORT SYNDROME WITHOUT HEMATURIA (CASE REPORT). IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD), 8(3), 250-251. SID. https://sid.ir/paper/309411/en

    Vancouver: Copy

    YIN YIN CHEN, YOU MING PENG, YU MEI LIANG. DELAYED DIAGNOSIS OF ALPORT SYNDROME WITHOUT HEMATURIA (CASE REPORT). IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD)[Internet]. 2014;8(3):250-251. Available from: https://sid.ir/paper/309411/en

    IEEE: Copy

    CHEN YIN YIN, PENG YOU MING, and LIANG YU MEI, “DELAYED DIAGNOSIS OF ALPORT SYNDROME WITHOUT HEMATURIA (CASE REPORT),” IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD), vol. 8, no. 3, pp. 250–251, 2014, [Online]. Available: https://sid.ir/paper/309411/en

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