Literature DB >> 6434850

Organic acids in urine of patients with congenital lactic acidoses: an aid to differential diagnosis.

R A Chalmers.   

Abstract

The differential diagnosis of patients with apparent congenital lactic acidoses poses one of the most intractable problems in the study of patients with disorders of organic acid metabolism. An outline of the factors leading to a lactic acidosis, particularly in infants and young children, together with a brief review of the known causes of congenital lactic acidosis, are presented. Quantitative examination of the organic acids excreted by patients with proven enzyme deficiencies causing congenital lactic acidosis has demonstrated the characteristic patterns that are associated with specific disorders of this kind. After exclusion of uninherited, acquired and secondary metabolic causes of lactic acidosis, the quantitative patterns of organic acid excretion, together with other clinical and biochemical observations, provide valuable indicators of the area of the underlying primary metabolic disorder for subsequent selected, confirmatory, enzymology. The study of organic acids has a key and central role in the approach to the clinical and biochemical investigation and diagnosis of patients with congenital lactic acidoses.

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Year:  1984        PMID: 6434850     DOI: 10.1007/bf03047380

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  28 in total

1.  Studies on a patient with in vivo evidence of type I glycogenosis and normal enzyme activities in vitro.

Authors:  R A Chalmers; B E Ryman; R W Watts
Journal:  Acta Paediatr Scand       Date:  1978-03

2.  Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles.

Authors:  J P Van Biervliet; L Bruinvis; D Ketting; P K De Bree; C Van der Heiden; S K Wadman
Journal:  Pediatr Res       Date:  1977-10       Impact factor: 3.756

3.  Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh's disease.

Authors:  B M Atkin; N R Buist; M F Utter; A B Leiter; B Q Banker
Journal:  Pediatr Res       Date:  1979-02       Impact factor: 3.756

4.  Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency.

Authors:  F X Coude; H Ogier; C Marsac; A Munnich; C Charpentier; J M Saudubray
Journal:  Pediatrics       Date:  1981-12       Impact factor: 7.124

5.  Report of a patient with severe, chronic lactic acidaemia and pyruvate carboxylase deficiency.

Authors:  J P Van Biervliet; L Bruinvis; C van der Heiden; D Ketting; S K Wadman; J L Willemse; L A Monnens
Journal:  Dev Med Child Neurol       Date:  1977-06       Impact factor: 5.449

6.  Pyruvate dehydrogenase phosphatase deficiency: a cause of congenital chronic lactic acidosis in infancy.

Authors:  B H Robinson; W G Sherwood
Journal:  Pediatr Res       Date:  1975-12       Impact factor: 3.756

7.  Two cases of phosphoenolpyruvate carboxykinase deficiency.

Authors:  F A Hommes; K Bendien; J D Elema; H J Bremer; I Lombeck
Journal:  Acta Paediatr Scand       Date:  1976-03

8.  Absence of pyruvate decarboxylase activity in man: a cause of congenital lactic acidosis.

Authors:  D F Farrell; A F Clark; C R Scott; R P Wennberg
Journal:  Science       Date:  1975-03-21       Impact factor: 47.728

9.  A patient with pyruvate carboxylase deficiency in the liver: treatment with aspartic acid and thiamine.

Authors:  M G Baal; F J Gabreëls; W O Renier; F A Hommes; T H Gijsbers; K J Lamers; J C Kok
Journal:  Dev Med Child Neurol       Date:  1981-08       Impact factor: 5.449

10.  Studies on alpha-ketoglutaric aciduria in type I glycogenosis.

Authors:  H Kodama; S Okada; K Inui; T Yutaka; H Yabuuchi
Journal:  Tohoku J Exp Med       Date:  1980-08       Impact factor: 1.848

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  5 in total

1.  Pyruvate carboxylase deficiency in twins.

Authors:  M A Pollock; M Cumberbatch; M J Bennett; R G Gray; M Brand; K Hyland; P J Congdon; T Pitts-Tucker; S Gray
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

2.  Secondary inhibition of multiple NAD-requiring dehydrogenases in respiratory chain complex I deficiency: possible metabolic markers for the primary defect.

Authors:  M J Bennett; W G Sherwood; K M Gibson; A B Burlina
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

3.  Glycerol-3-phosphate excretion in fructose-1,6-diphosphatase deficiency.

Authors:  S Krywawych; G Katz; A M Lawson; S Wyatt; D P Brenton
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

4.  Neonatal pyruvate dehydrogenase deficiency with lipoate responsive lactic acidaemia and hyperammonaemia.

Authors:  D J Byrd; H P Krohn; L Winkler; C Steinborn; M Hadam; J Brodehl; D H Hunneman
Journal:  Eur J Pediatr       Date:  1989-04       Impact factor: 3.183

5.  Coenzyme A Restriction as a Factor Underlying Pre-Eclampsia with Polycystic Ovary Syndrome as a Risk Factor.

Authors:  Charlie Hodgman; Gulafshana Hafeez Khan; William Atiomo
Journal:  Int J Mol Sci       Date:  2022-03-03       Impact factor: 5.923

  5 in total

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