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D28G Mutation in Congenital Glucose-Galactose Malabsorption

Kianifar Hamid-Reza نويسنده , Talebi Saeed نويسنده , Tavakkol-Afshari Jalil نويسنده , Esmaili Mohammad نويسنده , Davachi Behrouz نويسنده , Brook Azam نويسنده

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Background: Congenital glucose-galactose malabsorption is a rare autosomal recessive disorder of the intestinal transport of glucose and galactose, leading to watery diarrhea, dehydration, failure to thrive, and early death. Methods: In this study, we analyzed D28G mutation in 16 family members of a patient with typical presentation of congenital glucose-galactose malabsorption with polymerase chain reaction-Restriction Fragment Length Polymorphism method. Results: Nine members of this family were heterozygous for D28G mutation. Conclusion: To the best of our knowledge this is the first report of D28G mutation in Iran. Moreover, this simple typical PCR-Restriction Fragment Length Polymorphism method, allows immediate identification of D28G mutation.

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