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Literature DB >> 10490532

Congenital nephrotic syndrome responsive to captopril and indometacin.

Abstract

Two children with congenital nephrotic syndrome are described (one with Finnish-type nephrosis, the other with diffuse mesangial sclerosis). Both children have had a prolonged and sustained clinical response with good physical health and normal growth patterns using captopril and indometacin as their sole treatment. No adverse effects have been noted. We recommend a trial of indometacin and captopril treatment in cases of congenital nephrotic syndrome.

Entities: Chemical Disease Species

Mesh：

Substances：

Year: 1999 PMID： 10490532 PMCID： PMC1718016 DOI： 10.1136/adc.81.2.174

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

5 in total

1. Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population.

Authors: A Fuchshuber; P Niaudet; O Gribouval; G Jean; M C Gubler; M Broyer; C Antignac
Journal: Pediatr Nephrol Date: 1996-04 Impact factor: 3.714

2. Angiotensin converting enzyme inhibitor does not reduce proteinuria in an infant with congenital nephrotic syndrome of the Finnish type.

Authors: R Birnbacher; E Förster; C Aufricht
Journal: Pediatr Nephrol Date: 1995-06 Impact factor: 3.714

3. Adequate clinical control of congenital nephrotic syndrome by enalapril.

Authors: S Guez; M Giani; M L Melzi; C Antignac; B M Assael
Journal: Pediatr Nephrol Date: 1998-02 Impact factor: 3.714

4. Successful treatment of Finnish congenital nephrotic syndrome with captopril and indomethacin.

Authors: A Pomeranz; B Wolach; J Bernheim; Z Korzets; J Bernheim
Journal: J Pediatr Date: 1995-01 Impact factor: 4.406

Review 5. Management of congenital nephrotic syndrome of the Finnish type.

Authors: C Holmberg; M Antikainen; K Rönnholm; M Ala Houhala; H Jalanko
Journal: Pediatr Nephrol Date: 1995-02 Impact factor: 3.714

5 in total

7 in total

Congenital nephrotic syndrome responsive to captopril and indometacin.

1. Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population.

2. Angiotensin converting enzyme inhibitor does not reduce proteinuria in an infant with congenital nephrotic syndrome of the Finnish type.

3. Adequate clinical control of congenital nephrotic syndrome by enalapril.

4. Successful treatment of Finnish congenital nephrotic syndrome with captopril and indomethacin.

Review 5. Management of congenital nephrotic syndrome of the Finnish type.

1. Long-term outcome of congenital nephrotic syndrome after kidney transplantation in Japan.

2. Management of congenital nephrotic syndrome.

3. Nephrotic syndrome in infancy can spontaneously resolve.

4. Glomerular structural factors in progression of congenital nephrotic syndrome.

5. Congenital nephrotic syndrome of the finnish type.

6. Long-term outcome of heavy proteinuria in patients under 2 years of age.

7. Congenital nephrotic syndrome with prolonged renal survival without renal replacement therapy.