Introduction: Celiac disease (CD) is defined as an autoimmune disease (AD) caused by gluten ingestion in genetically sensitive individuals. Several publications have demonstrated the increased risk of AD in patients with CD, both adults and children, which requires systematic research. Our study aimed to determine the prevalence of AD in 60 patients diagnosed with CD and to highlight risk factors that may contribute to the emergence of AD. Materials and methods: We collected medical data from all CD patients under 16 years of age who also had AD. Our study was conducted in the Gastroenterology-Hepatology and Pediatric Nutrition Unit of the Pediatrics Department of the Mohamed VI Hospital and University Center in Oujda, Morocco, during a seven-year period between January 2017 and January 2024. Results: We studied 60 patients with CD in our study. Eight patients (13%) had an associated AD. Their average age was eight years, with extremes varying between two and 15 years. AD was diagnosed before CD in six cases (75%), in parallel with CD in one patient (12.5%), while in only one case, it was diagnosed after CD (12.5%). All our patients had a single AD associated with CD. These ADs were mainly type 1 diabetes in seven cases and autoimmune thyroiditis in only one case. All our patients followed a gluten -free diet in addition to specific treatment for associated AD. Nevertheless, despite regular medical follow-up and targeted dietary advice for the management of CD and associated AD, three patients encountered difficulties in following the recommended diet. Conclusion: Younger patients with CD have an increased risk of hypothyroidism and insulin -dependent diabetes. These data necessitate improved surveillance to discover these illnesses as early as possible in order to optimize management and reduce related consequences.
机构:
Univ Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
Jensen, M. Kyle
;
Holmen, John
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机构:
Intermt Healthcare, Homer Warner Ctr Informat Res, Salt Lake City, UT USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
Holmen, John
;
Williams, Marc S.
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机构:
Geisinger Hlth Syst, Genom Med Inst, Danville, PA USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
Williams, Marc S.
;
Book, Linda S.
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机构:
Univ Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
Book, Linda S.
;
Guthery, Stephen L.
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机构:
Univ Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
机构:
Univ Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
Jensen, M. Kyle
;
Holmen, John
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h-index: 0
机构:
Intermt Healthcare, Homer Warner Ctr Informat Res, Salt Lake City, UT USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
Holmen, John
;
Williams, Marc S.
论文数: 0引用数: 0
h-index: 0
机构:
Geisinger Hlth Syst, Genom Med Inst, Danville, PA USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
Williams, Marc S.
;
Book, Linda S.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA
Book, Linda S.
;
Guthery, Stephen L.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USAUniv Utah, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT 84113 USA