Literature DB >> 7352874

Presenile cataract formation and decreased activity of galactosemic enzymes.

H W Skalka, J T Prchal.   

Abstract

One hundred forty-seven patients, 144 with advanced cataract formation, had determinations of erythrocyte galactokinase and galactose-1-phosphate uridyl transferase performed. Significant reduction (more than 2 SDs) of one of these enzymes was found in 47.4% of patients 50 years old or less with presenile "idiopathic" bilateral cataracts, 7.1% of other patients with cataracts aged 50 years or less, and 3.8% of patients with cataracts aged 51 years or more. The differences between the group with presenile idiopathic cataracts and the other groups were statistically highly significant (P less than .001). Patients with reduced activity of galactokinase or galactose-1-phosphate uridyl transferase (presumed heterozygotes) compose about 1% of the general population, appear to be more susceptible to idiopathic presenile cataract formation, and may be more prone to secondary cataract formation after a variety of lenticular insults. Dietary restriction of milk and milk products may prevent or delay cataract formation in these individuals.

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Year:  1980        PMID: 7352874     DOI: 10.1001/archopht.1980.01020030265003

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  13 in total

1.  A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in Asians.

Authors:  Y Okano; M Asada; A Fujimoto; A Ohtake; K Murayama; K J Hsiao; K Choeh; Y Yang; Q Cao; J K Reichardt; S Niihira; T Imamura; T Yamano
Journal:  Am J Hum Genet       Date:  2001-02-23       Impact factor: 11.025

2.  Cataracts in children with classical galactosaemia and in their parents.

Authors:  J P Burke; M O'Keefe; R Bowell; E R Naughten
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

3.  Idiopathic presenile cataract formation and galactosaemia.

Authors:  R E Stevens; M B Datiles; S K Srivastava; N H Ansari; A E Maumenee; W J Stark
Journal:  Br J Ophthalmol       Date:  1989-01       Impact factor: 4.638

4.  Galactosemic enzyme levels in presenile cataracts.

Authors:  G Maraini; E Leardi; G Nuzzi
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1982       Impact factor: 3.117

5.  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

6.  Galactose intolerance and the risk of cataract.

Authors:  A F Winder; P Fells; R B Jones; R D Kissun; I S Menzies; J N Mount
Journal:  Br J Ophthalmol       Date:  1982-07       Impact factor: 4.638

7.  The relationship between glucose-6-phosphate dehydrogenase deficiency and cataracts in Sardinia. An epidemiological and biochemical study.

Authors:  N Orzalesi; M Fossarello; R Sorcinelli; U Schlich
Journal:  Doc Ophthalmol       Date:  1984-05-30       Impact factor: 2.379

8.  Mutations in galactose-1-phosphate uridyltransferase gene in patients with idiopathic presenile cataract.

Authors:  N Karas; L Gobec; V Pfeifer; B Mlinar; T Battelino; J Lukac-Bajalo
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 9.  Genetics of human cataract.

Authors:  A Shiels; J F Hejtmancik
Journal:  Clin Genet       Date:  2013-06-10       Impact factor: 4.438

Review 10.  Biology of Inherited Cataracts and Opportunities for Treatment.

Authors:  Alan Shiels; J Fielding Hejtmancik
Journal:  Annu Rev Vis Sci       Date:  2019-09-15       Impact factor: 6.422

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