菲薄基底膜病 thin glomerular basement membrane disease

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1. 菲薄基底膜腎症（良性家族性血尿） thin basement membrane nephropathy benign familial hematuria
2. 弧発性および持続性糸球体性血尿：IgA腎症、アルポート症候群、菲薄基底膜腎症 isolated and persistent glomerular hematuria iga alport thin basement membrane nephropathy
3. 小児における顕微鏡的血尿の評価 evaluation of microscopic hematuria in children
4. 糸球体疾患の鑑別診断および評価 differential diagnosis and evaluation of glomerular disease
5. 遺伝性腎炎（アルポート症候群）の遺伝学、病因、および病理 genetics pathogenesis and pathology of hereditary nephritis alport syndrome

English Journal

The association of IgA glomerulonephritis and thin glomerular basement membrane disease in a hematuric patient: light and electron microscopic and immunofluorescence investigation.

Monga G1, Mazzucco G, Roccatello D.
American journal of kidney diseases : the official journal of the National Kidney Foundation.Am J Kidney Dis.1991 Sep;18(3):409-12.
A double glomerulopathy (IgA glomerulonephritis [IgAGN] associated with thin glomerular basement membrane disease [TGBMD]) is reported in a 39-year-old woman presenting with macroscopic-microscopic hematuria. Her 3-year-old daughter was also affected by microhematuria of probable glomerular origin.
PMID 1882838

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