Literature DB >> 7093182

Galactose intolerance and the risk of cataract.

A F Winder, P Fells, R B Jones, R D Kissun, I S Menzies, J N Mount.   

Abstract

Cataracts may arise in association with various major and minor disorders restricting galactose metabolism, and the risk is broadly associated with the degree of galactose intolerance. A family is described in which a girl presented at the age of 7 3/4 years with cataracts, galactosuria, and partial deficiencies of the enzymes galactokinase and galactose-1-phosphate uridyl transferase. Galactose intolerance as determined by an oral test was impaired and fluctuated with variation in activity of the above galactose enzymes. Minor defects were also present in the parents and a maternal half-brother. The child has a compound disorder of galactose metabolism differing from those previously described. Assessment of galactose tolerance may be useful in the investigation of families with an incidence of cataract.

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Year:  1982        PMID: 7093182      PMCID: PMC1039818          DOI: 10.1136/bjo.66.7.438

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  22 in total

1.  Rennes-like variant of galactosemia: clinical and biochemical studies.

Authors:  G Hammersen; S Houghton; H L Levy
Journal:  J Pediatr       Date:  1975-07       Impact factor: 4.406

2.  Maternal enzymes of galactose metabolism and the "inexplicable" infantile cataract.

Authors:  J D Harley; P Mutton; S Irvine; J D Gupta
Journal:  Lancet       Date:  1974-08-03       Impact factor: 79.321

3.  A rapid simplified assay for galactokinase activity in whole blood.

Authors:  E Beutler; F Matsumoto
Journal:  J Lab Clin Med       Date:  1973-11

4.  Deficiency of uridine diphosphate galactose 4-epimerase in blood cells of an apparently healthy infant. Preliminary communication.

Authors:  R Gitzelmann
Journal:  Helv Paediatr Acta       Date:  1972-06

5.  Galactokinase deficiency and cataracts.

Authors:  N S Levy; A E Krill; E Beutler
Journal:  Am J Ophthalmol       Date:  1972-07       Impact factor: 5.258

6.  Partial galactose-1-phosphate uridyltransferase deficiency due to a variant enzyme.

Authors:  R Gitzelmann; J R Poley; A Prader
Journal:  Helv Paediatr Acta       Date:  1967-07

7.  Galactose tolerance studies of individuals with reduced galactose pathway activity.

Authors:  W J Mellman; B E Rawnsley; C W Nichols; B Needelman; M T Mennuti; J Malone; T A Tedesco
Journal:  Am J Hum Genet       Date:  1975-11       Impact factor: 11.025

8.  Improved method for measuring galactose-I-phosphate uridyl transferase activity of erythrocytes.

Authors:  E Beutler; M C Baluda
Journal:  Clin Chim Acta       Date:  1966-03       Impact factor: 3.786

9.  Excretion of galactitol in the urine of heterozygotes of both forms of galactosemia.

Authors:  F C Sitzmann; R D Schmid; H Kaloud
Journal:  Clin Chim Acta       Date:  1977-03-01       Impact factor: 3.786

10.  Biokinetics of galactose in the homozygotes and heterozygotes of both forms of galactosemia.

Authors:  F C Sitzmann; H Kaloud
Journal:  Clin Chim Acta       Date:  1976-11-01       Impact factor: 3.786

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  1 in total

1.  Partial galactose disorders in families with premature cataracts.

Authors:  A F Winder; L J Claringbold; R B Jones; B S Jay; N S Rice; R D Kissun; I S Menzies; J N Mount
Journal:  Arch Dis Child       Date:  1983-05       Impact factor: 3.791

  1 in total

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