Literature DB >> 3023748

Fructose-1,6-diphosphatase deficiency: diagnosis using leukocytes and detection of heterozygotes with radiochemical and spectrophotometric methods.

D Alexander, M Assaf, A Khudr, I Haddad, A Barakat.   

Abstract

The first two cases of fructose-1,6-diphosphatase (FDPase) deficiency from the Middle East have been diagnosed on leukocytes using a spectrophotometric assay and a new radiochemical technique. The control mean for FDPase measured by the spectrophotometric assay was 178.2 nm mg-1 h-1 (n = 12), 66.8 nm mg-1 h-1 for obligate heterozygotes (n = 4) and non-detectable in the two patients. By the radiochemical assay the values were controls, 103.3; heterozygotes, 20.6; patients, 0.46 and 3.5 nm mg-1 h-1. Using both methods it was possible to identify two certain FDPase heterozygotes and three non-carriers in the family of one of the probands. The radiochemical method was found to be more effective in differentiating heterozygotes from controls than the spectrophotometric method. However, either technique may be conveniently used for the diagnosis of FDPase deficiency in leukocytes.

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Year:  1985        PMID: 3023748     DOI: 10.1007/bf01805429

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


  10 in total

1.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

2.  Letter: FDPase activity in human leukocytes.

Authors:  J Cahill; M E Kirtley
Journal:  N Engl J Med       Date:  1975-01-23       Impact factor: 91.245

3.  Recurrent attacks of ketotic acidosis associated with fructose-1,6-diphosphatase deficiency.

Authors:  L Corbeel; E Eggermont; R Eeckels; J Jaeken; M Casteels-Van Daele; H Devlieger; B Delmontte
Journal:  Acta Paediatr Belg       Date:  1976 Jan-Mar

4.  Metabolic and biochemical studies in fructose 1,6-diphosphatase deficiency.

Authors:  S B Melancon; A K Khachadurian; H L Nadler; B I Brown
Journal:  J Pediatr       Date:  1973-04       Impact factor: 4.406

5.  Detection of fructose-1,6-diphosphatase deficiency with use of white blood cells.

Authors:  S B Melancon; H L Nadler
Journal:  N Engl J Med       Date:  1972-03-30       Impact factor: 91.245

6.  Fasting hypoglycaemia and metabolic acidosis associated with deficiency of hepatic fructose-1,6-diphosphatase activity.

Authors:  L Baker; A I Winegrad
Journal:  Lancet       Date:  1970-07-04       Impact factor: 79.321

7.  Five related Lebanese individuals with high plasma lysosomal hydrolases: a new defect in mannose-6-phosphate receptor recognition?

Authors:  D Alexander; G Dudin; F Talj; F Bitar; M Deeb; A Khudr; M Abboud; V M Der Kaloustian
Journal:  Am J Hum Genet       Date:  1984-09       Impact factor: 11.025

8.  A new radiochemical assay for fructose-1,6-diphosphatase in human leucocytes.

Authors:  A J Janssen; F J Trijbels
Journal:  Clin Chim Acta       Date:  1982-02-26       Impact factor: 3.786

9.  Deficiency of glucose-6-phosphate dehydrogenase found in a case of hepatic fructose-1,6-diphosphatase deficiency.

Authors:  A Kinugasa; T Kusunoki; A Iwashima
Journal:  Pediatr Res       Date:  1979-12       Impact factor: 3.756

10.  Genetic diseases in Lebanon.

Authors:  V M Der Kaloustian; J Naffah; J Loiselet
Journal:  Am J Med Genet       Date:  1980
  10 in total
  4 in total

1.  Biochemical and clinical observations in four patients with fructose-1,6-diphosphatase deficiency.

Authors:  P Bührdel; H J Böhme; L Didt
Journal:  Eur J Pediatr       Date:  1990-05       Impact factor: 3.183

2.  A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.

Authors:  Ghunwa Nakouzi; Khalil Kreidieh; Soha Yazbek
Journal:  J Community Genet       Date:  2014-09-27

3.  Diagnosis of fructose-1,6-bisphosphatase deficiency using leukocytes: normal leukocyte enzyme activity in three female patients.

Authors:  Y S Shin
Journal:  Clin Investig       Date:  1993-02

Review 4.  Human Metabolic Enzymes Deficiency: A Genetic Mutation Based Approach.

Authors:  Swati Chaturvedi; Ashok K Singh; Amit K Keshari; Siddhartha Maity; Srimanta Sarkar; Sudipta Saha
Journal:  Scientifica (Cairo)       Date:  2016-03-09
  4 in total

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