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Information Journal Paper

Title

An Unusual Case of Familial Systemic Lupus Erythematosus with Distal Renal Tubular Acidosis and Hemolytic Anemia

Pages

  337-339

Abstract

Systemic lupus erythematosus (SLE) in children is associated with renal involvement in majority of cases. While glomerular involvement is a common manifestation, tubular involvement is rare. Tubular dysfunctions previously described with SLE are renal tubular acidosis (Type 1 and less commonly type 4). Isolated renal tubular acidosis without glomerular involvement has not been reported in childhood SLE. We report an adolescent girl with SLE, autoimmune thyroiditis and distal RTA who subsequently developed autoimmune hemolytic anemia. During a follow-up of almost 7 years the girl never developed any proteinuria while the RTA persisted. Also during this period, her mother was diagnosed with SLE manifesting with thrombocytopenia.

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    APA: Copy

    Agrwal, Shipra, Mantan, Mukta, & Dabas, Aashima. (2019). An Unusual Case of Familial Systemic Lupus Erythematosus with Distal Renal Tubular Acidosis and Hemolytic Anemia. IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD), 13(5), 337-339. SID. https://sid.ir/paper/762405/en

    Vancouver: Copy

    Agrwal Shipra, Mantan Mukta, Dabas Aashima. An Unusual Case of Familial Systemic Lupus Erythematosus with Distal Renal Tubular Acidosis and Hemolytic Anemia. IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD)[Internet]. 2019;13(5):337-339. Available from: https://sid.ir/paper/762405/en

    IEEE: Copy

    Shipra Agrwal, Mukta Mantan, and Aashima Dabas, “An Unusual Case of Familial Systemic Lupus Erythematosus with Distal Renal Tubular Acidosis and Hemolytic Anemia,” IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD), vol. 13, no. 5, pp. 337–339, 2019, [Online]. Available: https://sid.ir/paper/762405/en

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