Literature DB >> 4006335

Asymptomatic low molecular weight proteinuria: a report on 5 cases.

Y Suzuki, T Okada, A Higuchi, D Mase, O Kobayashi.   

Abstract

In children with asymptomatic proteinuria, a high proportion of low molecular weight (LMW) proteins is an indicator of tubular malfunction. In a routine screening program covering the last 15 years and involving 280,000 children, aged between 3 and 19 years, we have identified 5 boys with LMW proteinuria. In 4 of these, renal biopsy was histologically normal on the first presentation. Follow-up for 4-16 years showed normal growth curves, but further evidence of tubular dysfunction appeared: glycosuria and hypophosphatemia in 2 patients; one of them had also aminoaciduria and rising serum creatinine (greater than 1.2 mg/100 ml). Another patient had only increased serum creatinine. The other two, still less than 13 years old, show so far no other abnormality than persistent LMW proteinuria. It is suggested that early identification of LMW proteinuria may presage gradual development of progressive tubular dysfunction with age and that such patients should be followed up indefinitely.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 4006335

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


  6 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.  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

3.  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

Review 4.  Low molecular weight proteins in children with renal disease.

Authors:  P A Tomlinson
Journal:  Pediatr Nephrol       Date:  1992-11       Impact factor: 3.714

5.  Urinary excretion of beta-2-microglobulin in patients with active metabolic stone disease.

Authors:  D Musialik
Journal:  Int Urol Nephrol       Date:  1989       Impact factor: 2.370

6.  Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq).

Authors:  Yuhong Ye; Jingjing Wang; Xiaofang Quan; Ke Xu; Haidong Fu; Weiyue Gu; Jianhua Mao
Journal:  BMC Nephrol       Date:  2020-05-11       Impact factor: 2.388

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.