Literature DB >> 2437388

HPRT-deficiency associated with normal PRPP concentration and APRT activity.

R B Gordon, D T Keough, B T Emmerson.   

Abstract

Deficiencies of HPRT are usually associated with increased concentrations of PRPP and increased levels of APRT activity in erythrocytes. We report the case of a male with a partial deficiency of HPRT in whom these two parameters were normal. The clinical features of this patient were those associated with severe hyperuricaemia and gout. Studies of intact erythrocytes showed rates of incorporation of [14C]hypoxanthine and of [14C]adenine into purine nucleotides which were almost indistinguishable from normal. However, HPRT activity in erythrocyte lysates was only 9% of normal. In cell extracts of cultured lymphoblasts, the HPRT activity was 20% of control values and the APRT activity was normal. The PRPP concentration and the rate of de novo purine synthesis in cultured lymphoblasts were both intermediate between controls and lymphoblasts from patients with the Lesch-Nyhan syndrome.

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Year:  1987        PMID: 2437388     DOI: 10.1007/bf01799493

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


  21 in total

1.  The enzymatic spectrophotometric method for determination of uric acid.

Authors:  L LIDDLE; J E SEEGMILLER; L LASTER
Journal:  J Lab Clin Med       Date:  1959-12

2.  Erythrocyte phosphoribosylpyrophosphate concentrations in heterozygotes for hypoxanthine-guanine phosphoribosyltransferase deficiency.

Authors:  R B Gordon; L Thompson; B T Emmerson
Journal:  Metabolism       Date:  1974-10       Impact factor: 8.694

3.  Simpler method for the determination of 5-phosphoribosyl-1-pyrophosphate in red blood cells.

Authors:  O Sperling; G Eilam; S Persky-Brosh; A De Vries
Journal:  J Lab Clin Med       Date:  1972-06

4.  The spectrum of hypoxanthine-guanine phosphoribosyltransferase deficiency.

Authors:  B T Emmerson; L Thompson
Journal:  Q J Med       Date:  1973-04

5.  Elevated AMP pyrophosphorylase activity in congenital IMP pyrophosphorylase deficiencey (Lesch-Nyhan disease).

Authors:  C S Rubin; M E Balis; S Piomelli; P H Berman; J Dancis
Journal:  J Lab Clin Med       Date:  1969-11

6.  Partial HPRT deficiency : heterozygotes exhibit one cell population in intact cell assays.

Authors:  R B Gordon; L Thompson; B T Emmerson
Journal:  Adv Exp Med Biol       Date:  1977       Impact factor: 2.622

7.  Diagnostic evaluation of phosphoribosylpyrophosphate synthetase activities in hemolysates.

Authors:  M J Losman; S Hecker; S Woo; M A Becker
Journal:  J Lab Clin Med       Date:  1984-06

8.  Adenine phosphoribosyltransferase in patients with disorders of purine and pyrimidine metabolism.

Authors:  J M Wilson; P E Daddona; T Otoadese; W N Kelley
Journal:  J Lab Clin Med       Date:  1982-02

9.  Purine synthesis de novo in lymphocytes from patients with gout.

Authors:  R B Gordon; A C Counsilman; S M Cross; B T Emmerson
Journal:  Clin Sci (Lond)       Date:  1982-11       Impact factor: 6.124

10.  Urate kinetics in hypoxanthine-guanine phosphoribosyltransferase deficiency: their significance for the understanding of gout.

Authors:  B T Emmerson; R B Gordon; L A Johnson
Journal:  Q J Med       Date:  1976-01
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  1 in total

1.  Biochemical basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in nine families.

Authors:  D T Keough; R B Gordon; J de Jersey; B T Emmerson
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

  1 in total

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