Literature DB >> 6408303

Further observations in a case of uridine diphosphate galactose-4-epimerase deficiency with a severe clinical presentation.

M J Henderson, J B Holton, R MacFaul.   

Abstract

The red-cell concentrations of galactose-1-phosphate and uridine diphosphate galactose have been studied in relation to dietary galactose in a case of uridine diphosphate galactose-4-epimerase deficiency (McKusick 23035). Uridine diphosphate galactose accumulates rapidly in response to very small amounts of galactose but the concentration of galactose-1-phosphate increases proportionately to galactose intake. The significance of the observation is discussed with respect to the pathogenesis and treatment of the disease.

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Year:  1983        PMID: 6408303     DOI: 10.1007/BF02391187

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


  3 in total

1.  Enzymatic estimation of erythrocytic galactose-1-phosphate.

Authors:  H N KIRKMAN; E S MAXWELL
Journal:  J Lab Clin Med       Date:  1960-07

2.  Evidence for galactosaemia in utero.

Authors:  J T Allen; M Gillett; J B Holton; G S King; B R Pettit
Journal:  Lancet       Date:  1980-03-15       Impact factor: 79.321

3.  Galactosaemia: a new severe variant due to uridine diphosphate galactose-4-epimerase deficiency.

Authors:  J B Holton; M G Gillett; R MacFaul; R Young
Journal:  Arch Dis Child       Date:  1981-11       Impact factor: 3.791

  3 in total
  13 in total

1.  A Case Study of Monozygotic Twins Apparently Homozygous for a Novel Variant of UDP-Galactose 4'-epimerase (GALE) : A Complex Case of Variant GALE.

Authors:  Ying Liu; Kristi Bentler; Bradford Coffee; Juliet S Chhay; Kyriakie Sarafoglou; Judith L Fridovich-Keil
Journal:  JIMD Rep       Date:  2012-07-01

2.  Galactose Epimerase Deficiency: Expanding the Phenotype.

Authors:  Filipa Dias Costa; Sacha Ferdinandusse; Carla Pinto; Andrea Dias; Liesbeth Keldermans; Dulce Quelhas; Gert Matthijs; Petra A Mooijer; Luísa Diogo; Jaak Jaeken; Paula Garcia
Journal:  JIMD Rep       Date:  2017-03-01

3.  Development of a protocol for newborn screening for disorders of the galactose metabolic pathway.

Authors:  F G Bowling; A R Brown
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

4.  Generalised uridine diphosphate galactose-4-epimerase deficiency.

Authors:  J H Walter; R E Roberts; G T Besley; J E Wraith; M A Cleary; J B Holton; R MacFaul
Journal:  Arch Dis Child       Date:  1999-04       Impact factor: 3.791

5.  Studies of the V94M-substituted human UDPgalactose-4-epimerase enzyme associated with generalized epimerase-deficiency galactosaemia.

Authors:  T M Wohlers; J L Fridovich-Keil
Journal:  J Inherit Metab Dis       Date:  2000-11       Impact factor: 4.982

Review 6.  Galactose disorders: an overview.

Authors:  J B Holton
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

7.  Human UDP-galactose 4'-epimerase (GALE) is required for cell-surface glycome structure and function.

Authors:  Alex Broussard; Alyssa Florwick; Chelsea Desbiens; Nicole Nischan; Corrina Robertson; Ziqiang Guan; Jennifer J Kohler; Lance Wells; Michael Boyce
Journal:  J Biol Chem       Date:  2019-12-09       Impact factor: 5.157

8.  Identification and characterization of a mutation, in the human UDP-galactose-4-epimerase gene, associated with generalized epimerase-deficiency galactosemia.

Authors:  T M Wohlers; N C Christacos; M T Harreman; J L Fridovich-Keil
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

Review 9.  Galactose toxicity in animals.

Authors:  Kent Lai; Louis J Elsas; Klaas J Wierenga
Journal:  IUBMB Life       Date:  2009-11       Impact factor: 3.885

Review 10.  Galactosemia unsolved.

Authors:  S Segal
Journal:  Eur J Pediatr       Date:  1995       Impact factor: 3.183

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