Literature DB >> 3031364

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

S Krywawych, G Katz, A M Lawson, S Wyatt, D P Brenton.   

Abstract

A patient aged 23 months with fructose-1,6-diphosphatase deficiency is reported. This infant demonstrated an increased urine excretion of glycerol-3-phosphate during episodes of hypoglycaemia. The excretion of this compound has not previously been described in this disease or in those disorders associated with a deficiency in one of the other three gluconeogenic enzymes associated with hypoglycaemia. Its presence in the urine from patients may be useful in diagnosis.

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Year:  1986        PMID: 3031364     DOI: 10.1007/BF01800490

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


  6 in total

1.  Gluconeogenesis in infancy and childhood. III. Deficiency of the extramitochondrial form of hepatic phosphoenolpyruvate carboxykinase in a case of persistent neonatal hypoglycaemia.

Authors:  J Vidnes; O Sovik
Journal:  Acta Paediatr Scand       Date:  1976-05

2.  The quantitative extraction and gas-liquid chromatographic determination of organic acids in urine.

Authors:  R A Chalmers; R W Watts
Journal:  Analyst       Date:  1972-12       Impact factor: 4.616

3.  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

4.  Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings.

Authors:  J M Saudubray; C Marsac; C L Cathelineau; M Besson Leaud; J P Leroux
Journal:  Acta Paediatr Scand       Date:  1976-11

5.  Lactic acidaemia.

Authors:  B H Robinson; W G Sherwood
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

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

Authors:  R A Chalmers
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

  6 in total
  8 in total

1.  Clinical and biochemical observations on three cases of fructose-1,6-diphosphatase deficiency.

Authors:  A B Burlina; M Poletto; Y S Shin; F Zacchello
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Fructose-1,6-bisphosphatase deficiency: severe phenotype with normal leukocyte enzyme activity.

Authors:  G T Besley; J H Walter; M A Lewis; C R Chard; G M Addison
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

3.  Novel mutations in patients with fructose-1,6-bisphosphatase deficiency.

Authors:  B Herzog; U Wendel; A A Morris; K Eschrich
Journal:  J Inherit Metab Dis       Date:  1999-04       Impact factor: 4.982

4.  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

5.  Urinary sugar phosphates and related organic acids in fructose-1,6-diphosphatase deficiency.

Authors:  A Nakai; Y Shigematsu; Y Y Liu; Y Kikawa; M Sudo
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

6.  Group tests for selective screening of inborn errors of metabolism.

Authors:  M Duran; L Dorland; S K Wadman; R Berger
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

Review 7.  Hypoglycaemia Metabolic Gene Panel Testing.

Authors:  Arianna Maiorana; Francesca Romana Lepri; Antonio Novelli; Carlo Dionisi-Vici
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-29       Impact factor: 5.555

8.  A Japanese boy with fructose-1,6-bisphosphatase deficiency who had a novel FBP1 mutation (p.Phe90Val).

Authors:  Keiko Nagahara; Daisuke Ariyasu; Junko Igaki; Yuki Hasegawa; Yukihiro Hasegawa
Journal:  Clin Pediatr Endocrinol       Date:  2017-09-28
  8 in total

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