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Isolated short stature as a presentation of celiac disease in Saudi children
Asaad Mohamed Abdullah Assiri1
1Department of Pediatrics, College of Medicine and King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.
Insights
Celiac disease is a significant cause of short stature in Saudi children. Early diagnosis through antibody screening and biopsy, followed by a gluten-free diet, improves growth.
Area of Science:
- Pediatric Endocrinology
- Gastroenterology
- Genetics
Background:
- Short stature is a common pediatric concern.
- Celiac disease can present without typical gastrointestinal symptoms.
- Early diagnosis is crucial for growth recovery.
Purpose of the Study:
- To determine the prevalence of celiac disease in Saudi children with short stature.
- To evaluate if routine lab tests can indicate celiac disease.
- To assess the impact of a gluten-free diet on growth.
Main Methods:
- 91 Saudi children with short stature underwent extensive endocrine and biochemical assessments.
- Tests included antibody assays (anti-endomysial, anti-tissue transglutaminase), growth hormone, thyroid function, and intestinal biopsies.
- Biopsies were classified using the Oberhuber classification.
Main Results:
- Prevalence of celiac disease was 10.9% (10/91) with total villous atrophy.
- Potential celiac disease (mild villous atrophy) was found in 4.3% (5/91).
- All diagnosed children showed improved growth on a gluten-free diet.
Conclusions:
- Celiac disease is an important, often asymptomatic, cause of short stature in Saudi children.
- Recommend screening with anti-tissue transglutaminase and anti-endomysial antibodies, followed by biopsy.
- Gluten-free diet is essential for growth catch-up in affected children.
Abstract:
The aim of this study is to assess the prevalence of isolated short stature as a clinical presentation of celiac disease in Saudi Arab children and whether some of the routine laboratory tests performed to determine the cause of short stature could suggest the diagnosis of celiac disease. A total of 91 children with short stature were included in the study. Extensive endocrine and biochemical assessments, including total protein, serum albumin, calcium phosphate and alkaline phosphatase assays; renal function tests; coagulation profile; anti-endomysial antibodies and anti-tissue transglutaminase antibody, growth hormone, thyroid stimulating hormone, free-thyroxin (FT4) assays; stool tests for giardiasis; bone age; and endoscopic intestinal biopsies, were done for all children. Ten of the 91 children had positive intestinal biopsies in the form of total villous atrophy, an increase in crypt height, and an increase in intra-epithelial lymphocyte (IEL) numbers up to >40 IEL/100 EC (Type 3C) according to the Oberhuber classification, confirming the diagnosis of celiac disease. Five children had mild villous atrophy according to this classification (Type 3A), and they were considered to have potential celiac disease. Seventy-six children had normal intestinal biopsies. Therefore, the prevalence of celiac disease among Saudi children with short stature was 10.9%, and 4.3% of the children were diagnosed as having potential celiac disease. After confirming the diagnosis of celiac disease, all children were kept on a gluten-free diet and all of them showed improvement in their growth rate. We concluded that celiac disease is a very important cause of short stature in children without gastrointestinal complaints in Saudi Arabia. We highly recommend anti-tissue transglutaminase and anti-endomysial antibody screening tests, and a small bowel biopsy to confirm the diagnosis of celiac disease irrespective of the results of the antibody assays, in children with short stature in Saudi Arabia. Once the diagnosis is confirmed, children should be kept on a gluten-free diet so they can catch up their growth early before they develop permanent short stature.
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