Literature DB >> 2122118

Plasma polyol levels in patients with cataract.

C Jakobs1, A C Douwes, M Brockstedt, F Stellaard, W Endres, Y S Shin.   

Abstract

Galactitol and sorbitol concentrations in plasma were determined in patients (with or without cataract) in whom homo- or heterozygosity for galactokinase, galactose-1-phosphate uridyltransferase, systemic or peripheral UDP-galactose epimerase and sorbitol dehydrogenase deficiency was confirmed. For the above disorders it can be concluded that elevation of plasma polyols is not always related to the presence or absence of cataract. In all cases with cataract, however, the plasma galactitol or sorbitol levels were elevated. In another group of patients with unexplained congenital or infantile cataracts, but without apparent enzyme defects, mild to moderately elevated concentrations of plasma galactitol or sorbitol were found in about 45%. In 8% of this group the cataract and the elevated plasma galactitol concentration could possibly have been related to partial maternal enzyme deficiency. In all the other cases the elevated plasma polyol concentration remains unexplained but could indicate a further cause of cataract formation due to a hitherto unknown galactose or glucose metabolic aberration.

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Year:  1990        PMID: 2122118     DOI: 10.1007/bf01799509

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


  13 in total

1.  A simple assay for galactokinase using DEAE-cellulose column chromatography.

Authors:  Y S Shin-Buehring; M Osang; R Ziegler; J Schaub
Journal:  Clin Chim Acta       Date:  1977-01-03       Impact factor: 3.786

2.  Elevated plasma galactitol levels in patients with congenital cataracts without apparent enzyme defect.

Authors:  C Jakobs; A C Douwes; R Kok; A de Jong; W Endres; Y S Shin
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

3.  Sorbitol dehydrogenase deficiency in a family with congenital cataracts.

Authors:  Y S Shin; M Rieth; W Endres; P Haas
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

4.  Assay of UDP-galactose 4-epimerase.

Authors:  Y S Shin; A von Rucker; M Rieth; W Endres
Journal:  Clin Chem       Date:  1982-11       Impact factor: 8.327

Review 5.  Galactose and cataract.

Authors:  D Stambolian
Journal:  Surv Ophthalmol       Date:  1988 Mar-Apr       Impact factor: 6.048

6.  Direct and maternal aspects of the risk of cataract with partial disorders of galactose metabolism.

Authors:  A F Winder; A R Fielder; J N Mount; J S Menzies
Journal:  Clin Genet       Date:  1985-09       Impact factor: 4.438

7.  Stable isotope dilution analysis of galactitol in amniotic fluid: an accurate approach to the prenatal diagnosis of galactosemia.

Authors:  C Jakobs; T G Warner; L Sweetman; W L Nyhan
Journal:  Pediatr Res       Date:  1984-08       Impact factor: 3.756

8.  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

9.  Red blood cell sorbitol dehydrogenase deficiency in a family with cataracts.

Authors:  G Vaca; B Ibarra; M Bracamontes; D García-Cruz; J Sánchez-Corona; C Medina; C Wunsch; G González-Quiroga; J M Cantú
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

10.  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

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  8 in total

1.  UDPgalactose epimerase in lens and fibroblasts: activity expression in patients with cataracts and mental retardation.

Authors:  Y S Shin; G C Korenke; P Huppke; I Knerr; T Podskarbi
Journal:  J Inherit Metab Dis       Date:  2000-06       Impact factor: 4.982

Review 2.  Inherited metabolic diseases affecting the carrier.

Authors:  W Endres
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

Review 3.  Cataract and metabolic disease.

Authors:  W Endres; Y S Shin
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

4.  Lens sorbitol dehydrogenase deficiency in a patient with congenital cataract.

Authors:  V Vetter; Y S Shin
Journal:  Eur J Pediatr       Date:  1995-05       Impact factor: 3.183

5.  Membrane-bound sorbitol dehydrogenase in human red blood cells. Studies in normal subjects and in enzyme-deficient subjects with congenital cataracts.

Authors:  A Alvarez; A Martínez; B Ibarra; C Medina; M Bracamontes; J Perea; G Vaca
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

6.  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

7.  Early manifestation of cataract in a child heterozygous for classical galactosaemia and with diabetes mellitus type I: increased plasma mannitol concentration in cataract patients.

Authors:  Y S Shin; K Reiter; A Urban; B Lorenz; W Kiess
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

8.  Sequence of a cDNA encoding rice (Oryza sativa L.) leaf ferredoxin-NADP+ reductase.

Authors:  H Aoki; N Doyama; S Ida
Journal:  Plant Physiol       Date:  1994-04       Impact factor: 8.340

  8 in total

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