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Fibronectin Glomerulopathy: A Rare Autosomal Dominant Glomerular Disease 被引量:2

Fibronectin Glomerulopathy: A Rare Autosomal Dominant Glomerular Disease
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摘要 A 43-year-old female was admitted to the Department of Nephrology at Jinling Hospital (Nanjing,China) in January 2017 complaining of edema for 3 months with urine abnormalities.Her father had renal disease (with no biopsy performed) when he was 40 years old and died of uremia at 56 years old.Her mother and brother were healthy;however,her daughter and nephew (her brother's son) had slightly high microalbumin levels in routine urine screenings.Her daughter's urinary protein level was weakly positive,whereas her nephew's urinary protein level was negative. A 43-year-old female was admitted to the Department of Nephrology at Jinling Hospital (Nanjing,China) in January 2017 complaining of edema for 3 months with urine abnormalities.Her father had renal disease (with no biopsy performed) when he was 40 years old and died of uremia at 56 years old.Her mother and brother were healthy;however,her daughter and nephew (her brother's son) had slightly high microalbumin levels in routine urine screenings.Her daughter's urinary protein level was weakly positive,whereas her nephew's urinary protein level was negative.
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2017年第18期2261-2262,共2页 中华医学杂志(英文版)
关键词 Fibronectin Glomerulopathy MUTATION PROTEINURIA Fibronectin Glomerulopathy Mutation Proteinuria
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