Literature DB >> 6815376

Long-term management of inherited renal tubular disorders.

F Manz, K Schärer.   

Abstract

In inherited renal tubular disorders with isolated defects of tubular transport medical treatment is usually either not indicated or is simple and effective. In some inherited metabolic disorders with complex defects of renal tubular transport a specific therapy is known. For example, in galactosemia and hereditary fructose intolerance crude products may be restricted or in cases of Wilson's disease copper stores may be reduced. In idiopathic Fanconi syndrome, cystinosis, oculocerebrorenal syndrome and glycogenosis Fanconi-Bickel, a symptomatic replacement treatment based on supplementation of water, electrolytes and vitamin D has improved the non-uremic survival of these patients considerably within the last 20 years. For long-term management of inherited renal tubular disorders, treatment of tubular dysfunction, chronic renal failure, and involved extrarenal organs must be supported by genetic counseling and assistance for social integration.

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Year:  1982        PMID: 6815376     DOI: 10.1007/bf01715841

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  14 in total

1.  Effect of chronic salt and water loading on the tubular defects of a child with Fanconi syndrome (cystinosis).

Authors:  B S Arant; I Greifer; C M Edelmann; A Spitzer
Journal:  Pediatrics       Date:  1976-09       Impact factor: 7.124

2.  [Evaluation of the dietary treatment of cystinosis].

Authors:  H Schmidt; P Lutz; H Bickel
Journal:  Monatsschr Kinderheilkd       Date:  1973-05

3.  Nature's transplant in Fabry's disease.

Authors:  E Beutler
Journal:  Lancet       Date:  1979-07-28       Impact factor: 79.321

4.  Combined report on regular dialysis and transplantation of children in Europe, 1980.

Authors:  M Broyer; R A Donckerwolcke; F P Brunner; H Brynger; C Jacobs; P Kramer; N H Selwood; A J Wing; P H Blake
Journal:  Proc Eur Dial Transplant Assoc       Date:  1981

5.  Treatment of Wilson's disease with trientine (triethylene tetramine) dihydrochloride.

Authors:  J M Walshe
Journal:  Lancet       Date:  1982-03-20       Impact factor: 79.321

6.  Ineffectiveness of ascorbic acid therapy in nephropathic cystinosis.

Authors:  J A Schneider; J J Schlesselman; S A Mendoza; S Orloff; J G Thoene; W A Kroll; A D Godfrey; J D Schulman
Journal:  N Engl J Med       Date:  1979-04-05       Impact factor: 91.245

7.  Renal magnesium wasting, incomplete tubular acidosis, hypercalciuria and nephrocalcinosis in siblings.

Authors:  F Manz; K Schärer; P Janka; J Lombeck
Journal:  Eur J Pediatr       Date:  1978-06-20       Impact factor: 3.183

8.  Nephrotic syndrome during treatment with alpha-mercaptopropionylglycine.

Authors:  G Rizzoni; L Pavanello; N Dussini; L Chiandetti; G Zacchello
Journal:  J Urol       Date:  1979-09       Impact factor: 7.450

Review 9.  Arachidonic acid metabolism, prostaglandins and the kidney.

Authors:  D J Levenson; C E Simmons; B M Brenner
Journal:  Am J Med       Date:  1982-02       Impact factor: 4.965

10.  A family with a dominant form of idiopathic Fanconi syndrome leading to renal failure in adult life.

Authors:  A Patrick; J S Cameron; C S Ogg
Journal:  Clin Nephrol       Date:  1981-12       Impact factor: 0.975

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  1 in total

1.  Progression of chronic renal failure in a historical group of patients with nephropathic cystinosis. European Collaborative Study on Cystinosis.

Authors:  F Manz; N Gretz
Journal:  Pediatr Nephrol       Date:  1994-08       Impact factor: 3.714

  1 in total

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