Literature DB >> 6479121

Treatment of congenital hyperammonemias.

C Bachmann.   

Abstract

A rapid recognition of congenital hyperammonemia, a clear diagnostic workup and institution of a combined treatment without delay, by restriction of nitrogen supply, adequate caloric supply, substitution of missing metabolites, and use of alternate routes of nitrogen excretion will help to control hyperammonemic crises and improve the prognosis. For long-term treatment the use of essential amino acid mixtures and perhaps of antiserotoninergic agents is needed.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6479121     DOI: 10.1159/000469450

Source DB:  PubMed          Journal:  Enzyme        ISSN: 0013-9432


  5 in total

1.  Propionic acidaemia: clinical, biochemical and therapeutic aspects. Experience in 30 patients.

Authors:  W Lehnert; W Sperl; T Suormala; E R Baumgartner
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

2.  Excretion of hippuric acid during sodium benzoate therapy in patients with hyperglycinaemia or hyperammonaemia.

Authors:  B A Barshop; J Breuer; J Holm; J Leslie; W L Nyhan
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

3.  N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication.

Authors:  G Schubiger; C Bachmann; P Barben; J P Colombo; O Tönz; D Schüpbach
Journal:  Eur J Pediatr       Date:  1991-03       Impact factor: 3.183

4.  Liver pathology in a new congenital disorder of urea synthesis: N-acetylglutamate synthetase deficiency.

Authors:  A Zimmermann; C Bachmann; G Schubiger
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1985

5.  Formation and excretion of NH3----NH4+. New aspects of an old problem.

Authors:  S Silbernagl; D Scheller
Journal:  Klin Wochenschr       Date:  1986-09-15
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.