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Our Cases with Sucrase Isomaltase Deficiency | OMICS International | Abstract
ISSN: 2161-069X

Journal of Gastrointestinal & Digestive System
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Case Report

Our Cases with Sucrase Isomaltase Deficiency

Miray Karakoyun1*, Erhan Kilicoglu1, Yasemin Ozdemir Sahan1, Masallah Baran2, Fatih Unal2 and Sema Aydogdu2

1Ege University Department of Pediatrics, Pediatric Gastroenterology, Hepatology and Nutrition Division, Gaziantep Pediatric Hospital, Turkey

2Ege University Department of Pediatrics, Pediatric Cardiology Division, Tepecik Training Hospital, Turkey

*Corresponding Author:
Miray Karakoyun
Ege University Department of Pediatrics
Pediatric Gastroenterology
Hepatology and Nutrition Division
Gaziantep Pediatric Hospital, Turkey
Tel: 5058699691
E-mail: miraykarakoyun@hotmail.com

Received date: October 26, 2015 Accepted date: November 05, 2015 Published date: November 11, 2015

Citation: Karakoyun M, Kilicoglu E, Sahan YO, Baran M, Unal F, et al. (2015) Our Cases with Sucrase Isomaltase Deficiency. J Gastrointest Dig Syst 5:354. doi:10.4172/2161-069X.1000354

Copyright: © 2015 Karakoyun M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Objectives: Individuals affected with sucrase isomaltase deficiency are unable to digest sucrose-containing foods. Primary symptoms include watery diarrhea, abdominal discomfort and vomiting. Secondary symptoms include retarded growth and malnutrition. Nonspecific symptoms may lead to lengthy delays in diagnosis. The objective of this report is to describe the clinical presentation, diagnosis and treatment of five Turkish children with sucrase isomaltase deficiency. Methods: This is a series of three male and two female patients that presented to the Department of Pediatric Gastroenterology, Hepatology, and Nutrition at Ege University between 2008 and 2014. Results: Patient ages ranged from 6 months to 9 years and symptoms began after the introduction of food or formula into the diet at 1 week to 6 months of age. Presenting symptoms included growth retardation, decreased weight gain, watery diarrhea and vomiting. Four patients were previously misdiagnosed with GERD, celiac disease, lactose intolerance and food allergy but they did not respond to standard treatment. Routine clinical laboratory assessments including hematology, renal, thyroid and hepatic function, renal tubular function were normal. A detailed history revealed the association between the onset of illness and dietary changes leading to the diagnosis of congenital sucrase isomaltase deficiency. All five patients responded to treatment with sacrosidase oral solution. Conclusion: This is the first case series of pediatric patients with sucrase isomaltase deficiency in Turkey. The actual prevalence of the disease in Turkey is unknown, probably due incorrect diagnoses. Four of our patients were previously misdiagnosed with other gastrointestinal disorders leading to delayed treatment. We suggest that sucrase isomaltase deficiency should be considered in pediatric patients presenting with chronic watery diarrhea.

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