Clinical Profile of Hereditary Fructose Intolerance in Children

Author:

Bharadia Dr. Lalit

Publisher

Jaypee Brothers Medical Publishing

Reference8 articles.

1. 1. Schrodi SJ, DeBarber A, He M, Ye Z, Peissig P, Van Wormer JJ, et.al. Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data. Human genetics. 2015 Jun 1;134(6):659-69.

2. 2. Bouteldja N, Timson DJ. The biochemical basis of hereditary fructose intolerance. Journal of inherited metabolic disease. 2010 Apr;33(2):105-12.

3. 3. Li H, Byers HM, Diaz-Kuan A, Vos MB, Hall PL, Tortorelli S, et.al. Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas. Molecular genetics and metabolism. 2018 Apr 1;123 (4):428-32.

4. 4. Krawczy.ski M, Targo.ska B, Kostrzewa-Szymiec D, Walkowiak J, Cichy W. Congenital fructose intolerance diagnosed in a 13-yearold boy. Wiadomosci Lekarskie (Warsaw, Poland: 1960). 1994 Sep 1;47 (17-18):702-4.

5. 5. Yang TY, Chen HL, Ni YH, Hwu WL, Chang MH. Hereditary fructose intolerance presenting as Reye's-like syndrome: report of one case. Acta Paediatrica Taiwanica= Taiwan er ke yi xue hui za zhi. 2000 Jul 1;41 (4):218-20.

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