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Title page

Original Article 


Fructosuria in a Sudanese Family

Omer Karrar, Mohamed Ibrahim A. Omer, Mahboob Ilahi.


Abstract
A Sudanese family who has three boys affected with fructosuria is reported and discussed. The index case, a 10-year-old boy, presented with vague abdominal pain, periodic attacks of polyuria and a reducing sugar in his urine that did not react with glhcose oxidase. A sucrose load (50 g) lead to substantial excretion of fructose In the urine and to polyuria. The absence of classical symptoms of hereditary fructose intolerance suggests essential fructosuria as the most likely abnormality in this family.

Key words: Essential fructosuria, Child, Sudan


 
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How to Cite this Article
Pubmed Style

Karrar O, Omer MIA, Ilahi M. Fructosuria in a Sudanese Family.

Web Style

Karrar O, Omer MIA, Ilahi M. Fructosuria in a Sudanese Family. https://sudanjp.com//?mno=104444 [Access: June 24, 2024].

AMA (American Medical Association) Style

Karrar O, Omer MIA, Ilahi M. Fructosuria in a Sudanese Family.


Vancouver/ICMJE Style

Karrar O, Omer MIA, Ilahi M. Fructosuria in a Sudanese Family.


Harvard Style

Karrar, O., Omer, . M. I. A. & Ilahi, . M. (1984) Fructosuria in a Sudanese Family.


Turabian Style

Karrar, Omer, Mohamed Ibrahim A. Omer, and Mahboob Ilahi. 1984. Fructosuria in a Sudanese Family.


Chicago Style

Karrar, Omer, Mohamed Ibrahim A. Omer, and Mahboob Ilahi. "Fructosuria in a Sudanese Family."


MLA (The Modern Language Association) Style

Karrar, Omer, Mohamed Ibrahim A. Omer, and Mahboob Ilahi. "Fructosuria in a Sudanese Family."


APA (American Psychological Association) Style

Karrar, O., Omer, . M. I. A. & Ilahi, . M. (1984) Fructosuria in a Sudanese Family.




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