WordNet

the presence of blood in the urine; often a symptom of urinary tract disease (同)haematuria

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Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome.

Gross O1, Kashtan CE2, Rheault MN2, Flinter F3, Savige J4, Miner JH5, Torra R6, Ars E6, Deltas C7, Savva I7, Perin L8, Renieri A9, Ariani F9, Mari F9, Baigent C10, Judge P10, Knebelman B11, Heidet L12, Lagas S13, Blatt D14, Ding J15, Zhang Y15, Gale DP16, Prunotto M17, Xue Y18, Schachter AD19, Morton LC20, Blem J21, Huang M21, Liu S22, Vallee S23, Renault D24, Schifter J25, Skelding J26, Gear S26, Friede T27, Turner AN28, Lennon R29.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.Nephrol Dial Transplant.2016 May 10. pii: gfw095. [Epub ahead of print]
Alport syndrome (AS) is a genetic disease characterized by haematuric glomerulopathy variably associated with hearing loss and anterior lenticonus. It is caused by mutations in the COL4A3, COL4A4 or COL4A5 genes encoding the α3α4α5(IV) collagen heterotrimer. AS is rare, but it accounts for >1%
PMID 27190345

Yuste C1, Gutierrez E1, Sevillano AM1, Rubio-Navarro A1, Amaro-Villalobos JM1, Ortiz A1, Egido J1, Praga M1, Moreno JA1.
World journal of nephrology.World J Nephrol.2015 May 6;4(2):185-95. doi: 10.5527/wjn.v4.i2.185.
Haematuria was known as a benign hallmark of some glomerular diseases, but over the last decade, new evidences pointed its negative implications on kidney disease progression. Cytotoxic effects of oxidative stress induced by hemoglobin, heme, or iron released from red blood cells may account for the
PMID 25949932

[Alport's syndrome and benign familial haematuria: light and electron microscopic studies of the kidney].

Dimitrijević J, Todorović V, Aleksić A, Jovanović D, Pilcević D, Vignjević S, Mićić S, Jovanović D, Pilcević D, Kovacević Z, Hrvacević R, Maksić D, Brajusković G, Savić V, Bogdanović R.
Srpski arhiv za celokupno lekarstvo.Srp Arh Celok Lek.2008 Dec;136 Suppl 4:275-81.
INTRODUCTION: Hereditary nephropathy is clinically characterized by the familial occurrence in successive generations of progressive haematuric nephritis and neural hearing loss. Hereditary nephropathy of Alport's syndrome (AS) and benign familial (recurrent) haematuria (BFH) are morphologically cha
PMID 20804095