WordNet

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

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1. 糸球体疾患の鑑別診断および評価 differential diagnosis and evaluation of glomerular disease
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. 成人における血尿の原因および評価 etiology and evaluation of hematuria in adults
4. 腎生検の適応および合併症 indications for and complications of renal biopsy
5. 小児における肉眼的血尿の評価 evaluation of gross hematuria in children

Prospective study on the potential of RAAS blockade to halt renal disease in Alport syndrome patients with heterozygous mutations.

Stock J1, Kuenanz J1, Glonke N1, Sonntag J1, Frese J1, Tönshoff B2, Höcker B2, Hoppe B3, Feldkötter M3, Pape L4, Lerch C4, Wygoda S5, Weber M6, Müller GA1, Gross O7.
Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2017 Jan;32(1):131-137. Epub 2016 Jul 11.
BACKGROUND: Patients with autosomal or X-linked Alport syndrome (AS) with heterozygous mutations in type IV collagen genes have a 1-20 % risk of progressing to end-stage renal disease during their lifetime. We evaluated the long-term renal outcome of patients at risk of progressive disease (chronic
PMID 27402170

Outcomes of kidney transplantation in Alport syndrome compared with other forms of renal disease.

Kelly YP1, Patil A2, Wallis L2, Murray S3, Kant S4, Kaballo MA5, Casserly L5, Doyle B6, Dorman A6, O'Kelly P1, Conlon PJ1,2.
Renal failure.Ren Fail.2016 Dec 5:1-4. [Epub ahead of print]
INTRODUCTION: Alport syndrome is an inherited renal disease characterized by hematuria, renal failure, hearing loss and a lamellated glomerular basement membrane. Patients with Alport syndrome who undergo renal transplantation have been shown to have patient and graft survival rates similar to or be
PMID 27917694

MELAS Syndrome and Kidney Disease Without Fanconi Syndrome or Proteinuria: A Case Report.

Rudnicki M1, Mayr JA2, Zschocke J3, Antretter H4, Regele H5, Feichtinger RG2, Windpessl M6, Mayer G7, Pölzl G8.
American journal of kidney diseases : the official journal of the National Kidney Foundation.Am J Kidney Dis.2016 Dec;68(6):949-953. doi: 10.1053/j.ajkd.2016.06.027. Epub 2016 Sep 24.
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS syndrome) represents one of the most frequent mitochondrial disorders. The majority of MELAS cases are caused by m.3243A>G mutation in the mitochondrial MT-TL1 gene, which encodes the mitochondrial tRNALeu(UUR). Kid
PMID 27683045

北川清樹,古市賢吾,和田隆志
日本アフェレシス学会雑誌 33(2), 117-122, 2014-05-31
… Rapidly progressive glomerulonephritis (RPGN) is a clinical syndrome involving abrupt or insidious onset of hematuria, proteinuria, anemia and rapidly progressive renal failure. … Anti-neutrophil cytoplasmic antibodies (ANCA) and anti-glomerular basement membrane (GBM) antibodies are thought to be involved in the clinical condition of RPGN. …
NAID 110009823174

A Unique Case of γ-heavy Chain Deposition Disease Characterized by Concomitant Deposition of γ2 and γ4 Subclasses

Yin Guang,Wu Yan,Zeng Cai-Hong,Chen Hui-Ping,Liu Zhi-Hong
Internal Medicine 53(22), 2615-2618, 2014
… γ-HCDD is the predominant subtype and is characterized by glomerular and tubular deposition of a single γ-heavy chain subclass. … A 39-year-old woman presented with hypertension, nephrotic syndrome, anemia, microscopic hematuria and progressive renal dysfunction. … Electron microscopy revealed electron-dense deposits along the glomerular and tubular basement membranes. …
NAID 130004713251

Nephrotic Syndrome and End-stage Kidney Disease Accompanied by Bicytopenia due to Copper Deficiency

Sakamaki Yuichi,Goto Kei,Watanabe Yasuo,Takata Takuma,Yamazaki Hajime,Imai Naofumi,Ito Yumi,Narita Ichiei
Internal Medicine 53(18), 2101-2106, 2014
… A 69-year-old man presented with proteinuria and hematuria. … In patients with various types of glomerular injuries, the ceruloplasmin expression is known to be increased. …
NAID 130004687649