Congenital Anomalies and Childhood Celiac Disease: A Swedish Register-based Study.
Författare
Summary, in English
Previously, chromosomal anomalies, and to a lesser extent, other congenital anomalies have been associated with an increased risk of celiac disease (CD). We investigated these associations using a systematic approach. We identified all singleton children (792,401) born in Sweden between 1987 and 1993, and obtained cases of CD using the Swedish National Inpatient Registry. We applied COX regression models as well as sibling designs to study the association between congenital anomalies and childhood CD. We observed that anomalies of either face, neck, ear, heart, digestive tract or of chromosomes were associated with CD.
Avdelning/ar
Publiceringsår
2012
Språk
Engelska
Sidor
736-739
Publikation/Tidskrift/Serie
Journal of Pediatric Gastroenterology and Nutrition - Jpgn
Volym
55
Issue
6
Länkar
Dokumenttyp
Artikel i tidskrift
Förlag
Lippincott Williams & Wilkins
Ämne
- Pediatrics
Nyckelord
- child
- celiac disease
- congenital abnormalities
- epidemiology
- heart
- diseases
- risk factors
Status
Published
Forskningsgrupp
- Social Epidemiology
- Celiac Disease and Diabetes Unit
ISBN/ISSN/Övrigt
- ISSN: 1536-4801