scholarly journals Aldehyde Oxidase and Xanthine Dehydrogenase in aflacca Tomato Mutant with Deficient Abscisic Acid and Wilty Phenotype

1999 ◽  
Vol 120 (2) ◽  
pp. 571-578 ◽  
Author(s):  
Moshe Sagi ◽  
Robert Fluhr ◽  
S. Herman Lips
Author(s):  
Cristina Collazo Abal ◽  
Susana Romero Santos ◽  
Carmen González Mao ◽  
Emilio C. Pazos Lago ◽  
Francisco Barros Angueira ◽  
...  

Abstract Objectives Hereditary xanthinuria is a rare, autosomal and recessive disorder characterized by severe hypouricemia and increased xanthine excretion, caused by a deficiency of xanthine dehydrogenase/oxidase (XDH/XO, EC: 1.17.1.4/1.17.3.2) in type I, or by a deficiency of XDH/XO and aldehyde oxidase (AOX, EC: 1.2.3.1) in type II. Case presentation We describe a novel point mutation in the XDH gene in homozygosis found in a patient with very low serum and urine levels of uric acid, together with xanthinuria. He was asymptomatic but renal calculi were discovered during imaging. Additional cases were found in his family and dietary recommendations were made in order to prevent further complications. Conclusions Hereditary xanthinuria is an underdiagnosed pathology, often found in a routine analysis that shows hypouricemia. It is important for Laboratory Medicine to acknowledge how to guide clinicians in the diagnosis.


2000 ◽  
Vol 97 (23) ◽  
pp. 12908-12913 ◽  
Author(s):  
M. Seo ◽  
A. J. M. Peeters ◽  
H. Koiwai ◽  
T. Oritani ◽  
A. Marion-Poll ◽  
...  

2004 ◽  
Vol 135 (1) ◽  
pp. 325-333 ◽  
Author(s):  
Miguel González-Guzmán ◽  
David Abia ◽  
Julio Salinas ◽  
Ramón Serrano ◽  
Pedro L. Rodríguez

2015 ◽  
Vol 37 (10) ◽  
Author(s):  
F. C. O. Macedo ◽  
H. Dziubinska ◽  
K. Trebacz ◽  
R. F. Oliveira ◽  
R. A. Moral

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