مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

CASE REPORT: A RARE CASE OF APHALLIA WITH RIGHT KIDNEY HYPOPLASIA AND LEFT KIDNEY DYSPLASIA

Pages

  257-259

Abstract

 Aphallia or penile agenesis is an extremely rare congenital anomaly with an estimated incidence rate of 1 in 10 to 30 million births. We report A RARE CASE OF APHALLIA WITH RIGHT KIDNEY HYPOPLASIA AND LEFT KIDNEY DYSPLASIA in a 10-day old Iranian-Azeri male. The patient had creatinine rise and renal failure due to dysplastic left kidney and hypoplastic right kidney and expired on fifth day of admission. There were only six cases of renal malformation associated with aphallia in the literature review. Three of the cases were complicated by Potter sequence and one of them was accompanied by chronic renal failure. Our case had a unique presentation because of bilateral renal malformation and subsequent renal failure without the Potter sequence.

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    APA: Copy

    ASLANABADI, SAIED, ZARRINTAN, SINA, ABDOLLAHI, HABIB, RIKHTEGAR, REZA, BEHESHTIROUY, SAMAD, BADEBARIN, DAVOD, & BAKY FAHMY, MOHAMED A.. (2015). CASE REPORT: A RARE CASE OF APHALLIA WITH RIGHT KIDNEY HYPOPLASIA AND LEFT KIDNEY DYSPLASIA. ARCHIVES OF IRANIAN MEDICINE, 18(4), 257-259. SID. https://sid.ir/paper/281231/en

    Vancouver: Copy

    ASLANABADI SAIED, ZARRINTAN SINA, ABDOLLAHI HABIB, RIKHTEGAR REZA, BEHESHTIROUY SAMAD, BADEBARIN DAVOD, BAKY FAHMY MOHAMED A.. CASE REPORT: A RARE CASE OF APHALLIA WITH RIGHT KIDNEY HYPOPLASIA AND LEFT KIDNEY DYSPLASIA. ARCHIVES OF IRANIAN MEDICINE[Internet]. 2015;18(4):257-259. Available from: https://sid.ir/paper/281231/en

    IEEE: Copy

    SAIED ASLANABADI, SINA ZARRINTAN, HABIB ABDOLLAHI, REZA RIKHTEGAR, SAMAD BEHESHTIROUY, DAVOD BADEBARIN, and MOHAMED A. BAKY FAHMY, “CASE REPORT: A RARE CASE OF APHALLIA WITH RIGHT KIDNEY HYPOPLASIA AND LEFT KIDNEY DYSPLASIA,” ARCHIVES OF IRANIAN MEDICINE, vol. 18, no. 4, pp. 257–259, 2015, [Online]. Available: https://sid.ir/paper/281231/en

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