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REVIEW OF CELIAC DISEASE PRESENTATION IN A PEDIATRIC TERTIARY CENTRE
Gracinda Nogueira Oliveira1, Rajiv Mohan2, Andrew Fagbemi2
1Hospital Pediátrico de Coimbra, Portugal.
Insights
Pediatric celiac disease presents diversely, impacting gastrointestinal and nutritional status. Early diagnosis and gluten-free diet improve symptoms and growth in children.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Clinical Nutrition
Background:
- Celiac disease is an immune-mediated disorder with varied presentations, complicating diagnosis.
- Understanding these diverse characteristics is crucial for timely intervention.
Purpose of the Study:
- To identify epidemiological, clinical, laboratory, and histologic features of pediatric celiac disease at diagnosis and during follow-up.
- To characterize the disease spectrum in children.
Main Methods:
- Retrospective analysis of 159 children (ages 1-17) diagnosed between 2014-2016.
- Data collected from electronic medical records and clinical notes.
- Evaluation included clinical symptoms, family history, serology, histology, and growth parameters.
Main Results:
- Classical presentation in 60%, non-classical in 25%, subclinical in 10%.
- Common symptoms: abdominal pain (58%), diarrhea (43%). Deficiencies noted: low ferritin (63%), vitamin D (62%).
- Gluten-free diet led to complete (51%) or partial (49%) clinical improvement; 100% showed height increase and 96% weight gain.
Conclusions:
- Pediatric celiac disease exhibits diverse clinical manifestations requiring broad clinician awareness.
- Early diagnosis and treatment significantly improve symptoms and nutritional status in affected children.
Background:
Celiac disease is an immune-mediated disorder with a multiform presentation and therefore a challenging diagnosis.
Objective:
Our purpose is to identify the epidemiological, clinical, laboratory and histologic characteristics of children with celiac disease at diagnosis and on follow-up.
Methods:
Children with previously established or newly diagnosed celiac disease, admitted in a tertiary centre in a two-year period (2014-2016) were recruited. Data was collected retrospectively from electronic medical records and clinical notes, and subsequently analysed with SPSS version 20.0.
Results:
A total of 159 patients, out of 312, were included. Age ranged from 1 to 17 years (mean ± SD: 8.5±4.5 years, 69% girls). Disease presentation was classical in 60%, non-classical in 25%, subclinical in 10% and 5% classified as potential celiac disease. Non-classical and subclinical profiles had a higher mean age at presentation but not statistically significant (P-value 0.24). The most frequent gastrointestinal features at presentation were abdominal pain (58%), diarrhea (43%) and bloating (27%). A positive family history for celiac disease was present in 24% (n=35). We found anaemia in 23%, low ferritin in 63% and a moderate to severe deficiency of 25-hydroxyvitamin D in 62%. celiac disease -specific serologic testing and esophagogastroduodenoscopy were performed in 99%. Histology revealed modified Marsh 2 or 3 enteropathy in 94%, the remaining had normal histology but positive human leukocyte antigen typing. Clinical improvement at 12 months of gluten-free diet was complete in 51% and partial in 49%. IgA tTG normalized after 12-30 months of gluten-free diet in 45%. On growth assessment at diagnosis and after 12-28 months of gluten-free diet, 100% had height increase (mean ±SD: 7.11±4.43 cm) and 96% weight gain (mean ±SD: 5.60±4.91 kg).
Conclusion:
Our findings outline the diverse clinical presentations of pediatric celiac disease that should be considered irrespective of age. Increased clinician's awareness will enable an early diagnosis and treatment, with subsequent symptom and nutritional status improvement.
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