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DOI 10.15537/smj.2017.9.20808

Медицинская библиотека · Saudi medical journal · 2017

Celiac disease in Saudi children. Evaluation of clinical features and diagnosis.

Saeed Anjum, Assiri Asaad, Assiri Hebah, Ullah Anhar, Rashid Mohsin

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Аннотация

Objectives

To characterize the clinical presentations and diagnosis including serological tests and histopathological findings in children with celiac disease.

Methods

All children (less than 18 years) with confirmed celiac disease diagnosed over a 6 year period at a private tertiary care health care center in Riyadh,  Saudi Arabia were studied retrospectively. Information collected included demographics, clinical presentation and diagnostic modalities with serology and small intestinal histology reported by Marsh grading.

Results

A total of 59 children had confirmed celiac disease. Thirty (50.8%) were male. Median age was 8 years (range 1 to 16 years). The mean duration of symptoms before diagnosis was 2.3 (±1.5) years. Classical disease was present only in 30.5%, whereas 69.5% had either non-classical presentations or belonged to high risk groups for celiac disease such as those with type-1 diabetes, autoimmune thyroiditis, Down syndrome and siblings. Failure to thrive was the most common presentation followed by short stature, abdominal pain and chronic diarrhea. Anti-tissue transglutaminase antibody was positive in 91.5%, and titers were no different between those with classical and non-classical disease. All had Marsh-graded biopsy findings consistent with celiac disease.

Conclusion

Children with celiac disease usually present with non-classical features. A high index of suspicion needs to be maintained to consider this disorder in the diagnostic workup of pediatric patients. High risk group should be screened early to avoid complications associated with untreated celiac disease.

Для цитирования: Saeed Anjum, Assiri Asaad, Assiri Hebah, Ullah Anhar, Rashid Mohsin. Celiac disease in Saudi children. Evaluation of clinical features and diagnosis.. Saudi medical journal. 2017. DOI: 10.15537/smj.2017.9.20808.

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