Congenital sucrase–isomaltase deficiency in Türkiye; a single center experience-Reference-Cited by-同舟云学术

Congenital sucrase–isomaltase deficiency in Türkiye; a single center experience

Published:2024-03-08 Issue:6 Volume:59 Page:647-651
ISSN:0036-5521
Container-title:Scandinavian Journal of Gastroenterology
language:en
Short-container-title:Scandinavian Journal of Gastroenterology

Author:

Barut Doğan¹^ORCID,Kıran Taşcı Ezgi¹,Kunay Bora¹,Güven Burcu²,Aksoy Betül³,Çağan Appak Yeliz³,Karakoyun Miray¹^ORCID,Çetin Funda¹,Selimoğlu Ayşe⁴,Onay Huseyin⁵,Aydoğdu Sema¹

Affiliation:

1. Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition Disease, Medical School of Ege University, Izmir, Turkey

2. Department of Pediatric Gastroenterology Hepatology and Nutrition, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey

3. Department of Pediatric Gastroenterology, Hepatology, and Nutrition, Izmir Katip Çelebi University, İzmir, Turkey

4. Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition Disease, Medical School, Memorial Ataşehir/Bahçelievler Hospital, İstanbul, Turkey

5. Department of Medical Genetics, Ege University Hospital, Izmir, Turkey

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/00365521.2024.2324961

Reference12 articles.

1. Our Cases with Sucrase Isomaltase Deficiency

2. Sucrase-isomaltase Gene Variants in Patients With Abnormal Sucrase Activity and Functional Gastrointestinal Disorders

3. Functional variants in the sucrase–isomaltase gene associate with increased risk of irritable bowel syndrome

4. Prevalence of congenital sucrase-isomaltase deficiency in Turkey may be much higher than the estimates

5. Congenital sucrase–isomaltase deficiency: diagnostic challenges and response to enzyme replacement therapy