Related Experiment Video
Updated: Aug 18, 2026

Recognition of Epidermal Transglutaminase by IgA and Tissue Transglutaminase 2 Antibodies in a Rare Case of Rhesus Dermatitis
Published on: December 15, 2011
[Clinical picture of celiac disease in children]
Urszula Grzybowska-Chlebowczyk1, Halina Woś, Sabina Wiecek
1Klinika Pediatrii Slaskiej Akademii Medycznej, Górnoślaskie Centrum Zdrowia Dziecka i Matki w Katowicach. klinikapediatrii@ślam.katowice.pl
Insights
Celiac disease in children often presents with few or no symptoms, despite significant intestinal damage. Early diagnosis is crucial, even without clear clinical signs, to manage this gluten-induced autoimmune disorder.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Gastroenterology
Context:
- Celiac disease incidence is shifting towards asymptomatic and oligosymptomatic forms.
- Atypical presentations and extraintestinal manifestations are increasingly observed in children and adults.
- Clinical symptoms can manifest at any age, including latent forms triggered by various factors.
Purpose:
- To present the diverse clinical presentations of celiac disease in pediatric patients.
- To highlight the challenges in diagnosing celiac disease when typical symptoms are absent.
Summary:
- A study evaluated 16 children (12 months to 17 years) diagnosed with celiac disease via clinical, histopathological, and immunological methods.
- The most frequent diagnosis was silent, monosymptomatic celiac disease, with some presenting with growth retardation, osteoporosis, or anemia.
- Notably, 3 patients had gastrointestinal symptoms and histopathological changes but lacked immunological markers for celiac disease.
Impact:
- Celiac disease in school-aged children frequently lacks obvious clinical disorders despite significant histopathological abnormalities.
- This underscores the importance of considering celiac disease in pediatric patients with subtle or atypical symptoms.
- Highlights the diagnostic challenges posed by cases with discordant clinical, immunological, and histopathological findings.
Unlabelled:
During the last few years we have been observing the decreasing incidence of the symptomatic celiac disease and increasing incidence of mono- and asymptomatic disease. Various atypical symptoms and extraintestinal manifestations were observed in older children (above 7 years) and in adults. Clinical symptoms of celiac disease may appear at any age, in each of the following forms: clinical celiac disease (symptomatic), silent (oligosymptomatic) or latent, with late manifestation, being the effect of stress, pregnancy, infections or excessive dietary gluten provocation.
The Aim Of The Study:
The presentation the variety of clinical pictures of celiac disease in children.
Materials And Methods:
We have evaluated the clinical course of celiac disease in 16 children (13 girls and 3 boys), aged between 12 months to 17 years (mean-7,5 years). The celiac disease was diagnosed on the grounds of clinical symptoms, histopathological examination of the small intestinal endoscopic biopsy and immunological examinations: serum antitransglutaminase antibodies and anti-endomysium antibodies.
Results:
Most commonly diagnosed form was the silent, monosymptomatic celiac disease. Four children manifested with growth retardation, one with osteoporosis, and one with iron deficiency anemia resistant to treatment. Two girls (aged 16 and 17 years) presented with symptomatic celiac disease. In 3 patients despite the gastrointestinal symptoms and histopathological changes present (villous atrophy, Marsh's index > 40) we did not find any immunological markers of celiac disease (with normal IgA levels).
Conclusions:
School-aged children with celiac disease, in many cases have no evident clinical and functional disorders caused by gluten intake, despite to presence of considerable abnormalities in the histopathological examination.
Related Concept Videos
Giardiasis
Inflammatory Bowel Disease IV: Clinical Manifestations
Inflammatory Bowel Disease II: Crohn's Disease
Inflammatory bowel disease, commonly known as IBD, refers to a collection of disorders that lead to persistent inflammation of the gastrointestinal tract. The two types of IBD are ulcerative colitis, which impacts the colon, and Crohn's disease, which can involve any part of the gastrointestinal segment.
Crohn's disease
Crohn's disease is a chronic, systemic inflammatory bowel disease (IBD) that predominantly affects the gastrointestinal tract. It is marked by transmural...
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Inborn Errors of Metabolism
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes: