Literature DB >> 6436490

Favism: looking for an autosomal gene associated with glucose-6-phosphate dehydrogenase deficiency.

C Mareni, L Repetto, G Forteleoni, T Meloni, G F Gaetani.   

Abstract

Favism is a severe, acute haemolytic anaemia which occurs in about 20% of G6PD deficient subjects after ingestion of fava beans. Since not all G6PD deficient subjects are sensitive to fava beans, the possibility has been suggested that extra erythrocytic factors may play an important role in the susceptibility to haemolytic favism. To test the hypothesis that an autosomal enzyme is involved in the pathogenesis of favism, we carried out a beta-glucosidase assay in small intestine biopsies from normal subjects and G6PD deficient subjects with or without favism. Beta-glucosidase might be involved in the absorption and metabolism of fava beans and a quantitative polymorphism could explain the different susceptibility to fava beans of G6PD deficient subjects. Our observation showed no consistent quantitative polymorphism of beta-glucosidase in the subjects examined.

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Year:  1984        PMID: 6436490      PMCID: PMC1049297          DOI: 10.1136/jmg.21.4.278

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  14 in total

Review 1.  Inherited haemolytic states: glucose-6-phosphate dehydrogenase deficiency.

Authors:  L Luzzatto
Journal:  Clin Haematol       Date:  1975-02

2.  Urinary D-glucaric acid excretion in normal and G-6-PD-deficient children with favism.

Authors:  C Cassimos; K Malaka-Zafiriu; J Tsiures
Journal:  J Pediatr       Date:  1974-06       Impact factor: 4.406

3.  Favism: current problems and investigations.

Authors:  E Bottini
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

Review 4.  Glucose-6-phosphate dehydrogenase.

Authors:  H N Kirkman
Journal:  Adv Hum Genet       Date:  1971

5.  Favism: clinical and biochemical data.

Authors:  C A Kattamis; M Kyriazakou; S Chaidas
Journal:  J Med Genet       Date:  1969-03       Impact factor: 6.318

Review 6.  New developments in glucose-6-phosphate dehydrogenase deficiency.

Authors:  L Luzzatto
Journal:  Isr J Med Sci       Date:  1973 Sep-Oct

7.  On the familial predisposition to favism.

Authors:  G Stamatoyannopoulos; G R Fraser; A C Motulsky; P Fessas; A Akrivakis; T Papayannopoulou
Journal:  Am J Hum Genet       Date:  1966-05       Impact factor: 11.025

8.  The diagnosis of the adult type of Gaucher's disease and its carrier state by demonstration of deficiency of beta-glucosidase activity in peripheral blood leukocytes.

Authors:  E Beutler; W Kuhl
Journal:  J Lab Clin Med       Date:  1970-11

9.  Favism: association with erythrocyte acid phosphatase phenotype.

Authors:  E Bottini; P Lucarelli; R Agostino; R Palmarino; L Businco; G Antognoni
Journal:  Science       Date:  1971-01-29       Impact factor: 47.728

10.  The epidemiology of favism.

Authors:  M A Belsey
Journal:  Bull World Health Organ       Date:  1973       Impact factor: 9.408

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  3 in total

Review 1.  Glucose-6-phosphate dehydrogenase deficiency.

Authors:  A B Mehta
Journal:  Postgrad Med J       Date:  1994-12       Impact factor: 2.401

2.  Lactose absorption in patients with glucose 6-phosphate dehydrogenase deficiency with and without favism.

Authors:  T Meloni; C Colombo; A Ogana; M C Mannazzu; G F Meloni
Journal:  Gut       Date:  1996-08       Impact factor: 23.059

3.  Decreased erythrocyte nucleoside transport and hENT1 transporter expression in glucose 6-phosphate dehydrogenase deficiency.

Authors:  Mohammad Al-Ansari; James D Craik
Journal:  BMC Hematol       Date:  2015-12-19
  3 in total

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