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Information Journal Paper

Title

Collagenofibrotic Glomerulopathy: Report a Rare Case

Pages

  409-411

Abstract

 Collagenofibrotic glomerulopathy is a rare clinical entity with fewer than 40 cases reported worldwide. We describe a case of adult onset Nephrotic syndrome with partial villous atrophy of the intestine who was diagnosed with this rare entity. Collagenofibrotic glomerulopathy is characterized by subendothelial and mesangial collagen type III deposition and increased procollagen III peptide levels. Extra renal involvement has been described in the form of hypertension, anemia and microangiopathic hemolytic anemia but villous atrophy has not been associated with this condition so far, possibly reflecting the paucity of literature. We describe this case and review the condition in this report.

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  • Cite

    APA: Copy

    Agarwal, Rakesh, Baid, Rashmi, & Mukhopadhyay, Jotideb. (2020). Collagenofibrotic Glomerulopathy: Report a Rare Case. ARCHIVES OF IRANIAN MEDICINE, 23(6), 409-411. SID. https://sid.ir/paper/281975/en

    Vancouver: Copy

    Agarwal Rakesh, Baid Rashmi, Mukhopadhyay Jotideb. Collagenofibrotic Glomerulopathy: Report a Rare Case. ARCHIVES OF IRANIAN MEDICINE[Internet]. 2020;23(6):409-411. Available from: https://sid.ir/paper/281975/en

    IEEE: Copy

    Rakesh Agarwal, Rashmi Baid, and Jotideb Mukhopadhyay, “Collagenofibrotic Glomerulopathy: Report a Rare Case,” ARCHIVES OF IRANIAN MEDICINE, vol. 23, no. 6, pp. 409–411, 2020, [Online]. Available: https://sid.ir/paper/281975/en

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