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1. 重症蛋白尿およびネフローゼ症候群の概要 overview of heavy proteinuria and the nephrotic syndrome
2. 小児におけるネフローゼ症候群の病因、臨床症状、および診断 etiology clinical manifestations and diagnosis of nephrotic syndrome in children
3. 小児における特発性ネフローゼ症候群の治療 treatment of idiopathic nephrotic syndrome in children
4. ネフローゼ症候群患者における浮腫の病態生理学および治療 pathophysiology and treatment of edema in patients with the nephrotic syndrome
5. 先天性乳児ネフローゼ症候群 congenital and infantile nephrotic syndrome

English Journal

Szeto CC.
Clinica chimica acta; international journal of clinical chemistry.Clin Chim Acta.2014 Sep 25;436C:308-313. doi: 10.1016/j.cca.2014.06.016. Epub 2014 Jun 30.
Nephrotic syndrome is a common problem in clinical nephrology. In general, nephrotic syndrome is pathognomonic of glomerular disease, but the underlying pathological etiology is highly variable. Although kidney biopsy is the standard method to classify the histology and determine the extent of renal
PMID 24992527

Hogan J1, Radhakrishnan J2.
Advances in chronic kidney disease.Adv Chronic Kidney Dis.2014 Sep;21(5):434-441. doi: 10.1053/j.ackd.2014.03.016.
Focal segmental glomerulosclerosis (FSGS) is the histologic end point of many disease processes that affect the kidney. Clinically, adults with FSGS present with proteinuria that may be accompanied by the nephrotic syndrome. Once identifiable (secondary) causes are excluded, the diagnosis of idiopat
PMID 25168833

Pollak MR.
Advances in chronic kidney disease.Adv Chronic Kidney Dis.2014 Sep;21(5):422-425. doi: 10.1053/j.ackd.2014.06.001.
Focal segmental glomerulosclerosis (FSGS) and nephrotic syndrome can be caused by rare highly penetrant mutations in number of genes. FSGS can follow both recessive and dominant inheritance patterns. In general, recessive forms present early, whereas the autosomal dominant forms present in adolescen
PMID 25168831