Literature DB >> 3457521

Proximal renal tubular acidosis in a child with type 1 glycogen storage disease.

N Matsuo, Y Tsuchiya, H Cho, T Nagai, A Tsuji.   

Abstract

A 6 1/2-year-old Japanese girl with type 1 glycogen storage disease developed a profound metabolic acidosis refractory to bicarbonate renal tubular acidosis and hyperphosphaturia. There was no evidence of distal tubular dysfunction.

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Year:  1986        PMID： 3457521     DOI： 10.1111/j.1651-2227.1986.tb10210.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


  5 in total

1.  Renal function and kidney size in glycogen storage disease type I.

Authors:  W C Reitsma-Bierens; G P Smit; J A Troelstra
Journal:  Pediatr Nephrol       Date:  1992-05       Impact factor: 3.714

2.  Glomerular and tubular function in glycogen storage disease.

Authors:  P J Lee; R N Dalton; V Shah; P C Hindmarsh; J V Leonard
Journal:  Pediatr Nephrol       Date:  1995-12       Impact factor: 3.714

3.  Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy.

Authors:  Julie Clar; Blandine Gri; Julien Calderaro; Marie-Christine Birling; Yann Hérault; G Peter A Smit; Gilles Mithieux; Fabienne Rajas
Journal:  Kidney Int       Date:  2014-04-09       Impact factor: 10.612

Review 4.  Type I glycogen storage disease: kidney involvement, pathogenesis and its treatment.

Authors:  Y T Chen
Journal:  Pediatr Nephrol       Date:  1991-01       Impact factor: 3.714

5.  Metabolic control and renal dysfunction in type I glycogen storage disease.

Authors:  J I Wolfsdorf; L M Laffel; J F Crigler
Journal:  J Inherit Metab Dis       Date:  1997-08       Impact factor: 4.982
  5 in total

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