Literature DB >> 1689232

The clinical significance of asymptomatic low molecular weight proteinuria detected on routine screening of children in Japan: a survey of 53 patients.

T Murakami1, H Kawakami.   

Abstract

A nationwide questionnaire survey uncovered 53 patients with asymptomatic low molecular weight (LMW) proteinuria, 52 males and one female, aged 3 to 32 years. There was a slight tendency toward shortening stature with increasing age. Mild proteinuria was present in all of them, and microscopic hematuria was occasionally noted in one-fourth, while glucosuria or aminoaciduria was rare. The share of their urinary LMW proteins was increased as evidenced by an increase in the alpha-globulin fraction on cellulose-acetate membrane electrophoresis (27 patients) and/or by an increase in the LMW proteins on sodium dodecylsulfate-polyacrylamide gel electrophoresis (17 patients). Urinary beta 2-microglobulin, one of the LMW proteins, was measured and proved to be increased but electrophoretic analyses were not performed in 25 patients. Urinary N-acetyl-beta-D-glucosaminidase activity, an indicator of renal proximal tubular damage, was elevated in 31 of 38 patients studied: Histological studies of renal biopsies revealed focal changes: focal global sclerosis in seven and tubular atrophy and/or tubular casts in nine out of 32 patients studied.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 1689232

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  9 in total

1.  Frequency of elevated urinary beta 2-microglobulin levels in relatives of patients with asymptomatic low-molecular-weight proteinuria.

Authors:  H Kawakami; T Murakami; S Matsuyama
Journal:  Pediatr Nephrol       Date:  1991-05       Impact factor: 3.714

2.  Phenotype and genotype of Dent's disease in three Korean boys.

Authors:  Hae Il Cheong; Jung Won Lee; Shou Huan Zheng; Joo Hoon Lee; Ju Hyung Kang; Hee Gyung Kang; Il Soo Ha; Seung Joo Lee; Yong Choi
Journal:  Pediatr Nephrol       Date:  2005-02-18       Impact factor: 3.714

3.  A case of adult Dent disease in Japan with advanced chronic kidney disease.

Authors:  Ken Saida; Yuji Kamijo; Daisuke Matsuoka; Shunsuke Noda; Yoshihiko Hidaka; Tetsuo Mori; Hisashi Shimojo; Takashi Ehara; Kenichiro Miura; Junko Takita; Takashi Sekine; Takashi Igarashi; Kenichi Koike
Journal:  CEN Case Rep       Date:  2013-11-02

4.  A patient with nephrotic-range proteinuria and focal global glomerulosclerosis.

Authors:  Fernando C Fervenza
Journal:  Clin J Am Soc Nephrol       Date:  2013-07-25       Impact factor: 8.237

5.  Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).

Authors:  S E Lloyd; S H Pearce; W Günther; H Kawaguchi; T Igarashi; T J Jentsch; R V Thakker
Journal:  J Clin Invest       Date:  1997-03-01       Impact factor: 14.808

6.  Dent's disease: clinical features and molecular basis.

Authors:  Félix Claverie-Martín; Elena Ramos-Trujillo; Víctor García-Nieto
Journal:  Pediatr Nephrol       Date:  2010-10-10       Impact factor: 3.714

7.  Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?

Authors:  Yaacov Frishberg; Dganit Dinour; Ruth Belostotsky; Rachel Becker-Cohen; Choni Rinat; Sofia Feinstein; Paulina Navon-Elkan; Efrat Ben-Shalom
Journal:  Pediatr Nephrol       Date:  2009-12       Impact factor: 3.714

8.  The first Sri Lankan family with Dent disease-1 due to a pathogenic variant in the CLCN5 gene: a case report.

Authors:  Randula Ranawaka; Nirmala Dushyanthi Sirisena; Kavinda Chandimal Dayasiri; Andrea G Cogal; John C Lieske; Manoji Prabashini Gamage; Vajira H W Dissanayake
Journal:  BMC Res Notes       Date:  2017-10-30

9.  Two brothers with identical variants of the CLCN5 gene-one developing Dent's disease.

Authors:  Anne Sophie Fischer; Niels Marcussen; Maria Rasmussen; Else Randers
Journal:  Clin Kidney J       Date:  2017-10-16
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.