Exploring congenital sucrase-isomaltase deficiency in autism spectrum disorder patients with irritable bowel syndrome symptoms: A prospective SI gene sequencing study

Congenital sucrase-isomaltase deficiency (CSID) is an inherited metabolic disorder causing chronic gastrointestinal symptoms and malnutrition when untreated. Most CSID patients are likely to remain under- or misdiagnosed. This study aimed to investigate prevalence of CSID among patients with autism...

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Veröffentlicht in:Autism research 2024-12
Hauptverfasser: Zubarioglu, Tanyel, Ulgen, Dilara, Akca-Yesil, Sedanur, Akbulut, Selin, Onay, Huseyin, Uzunyayla-Inci, Gozde, Beser, Omer Faruk, Hatemi, Ali İbrahim, Aktuğlu-Zeybek, Çiğdem, Kiykim, Ertuğrul
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Sprache:eng
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