Congenital anomalies and childhood celiac disease in Sweden

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Standard

Congenital anomalies and childhood celiac disease in Sweden. / Clinical Sciences, Malmö, Lund University, Department; Agardh, Daniel; univers, Lund.

I: Journal of Pediatric Gastroenterology and Nutrition, Bind 55, Nr. 6, 12.2012, s. 736-9.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Clinical Sciences, Malmö, Lund University, D, Agardh, D & univers, L 2012, 'Congenital anomalies and childhood celiac disease in Sweden', Journal of Pediatric Gastroenterology and Nutrition, bind 55, nr. 6, s. 736-9. https://doi.org/10.1097/MPG.0b013e318269f19d

APA

Clinical Sciences, Malmö, Lund University, D., Agardh, D., & univers, L. (2012). Congenital anomalies and childhood celiac disease in Sweden. Journal of Pediatric Gastroenterology and Nutrition, 55(6), 736-9. https://doi.org/10.1097/MPG.0b013e318269f19d

Vancouver

Clinical Sciences, Malmö, Lund University D, Agardh D, univers L. Congenital anomalies and childhood celiac disease in Sweden. Journal of Pediatric Gastroenterology and Nutrition. 2012 dec.;55(6):736-9. https://doi.org/10.1097/MPG.0b013e318269f19d

Author

Clinical Sciences, Malmö, Lund University, Department ; Agardh, Daniel ; univers, Lund. / Congenital anomalies and childhood celiac disease in Sweden. I: Journal of Pediatric Gastroenterology and Nutrition. 2012 ; Bind 55, Nr. 6. s. 736-9.

Bibtex

@article{6925faaaa0854d789e37a23bae03f7c6,
title = "Congenital anomalies and childhood celiac disease in Sweden",
abstract = "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 of the 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 face, neck, ear, heart, digestive tract, or chromosomes were associated with CD.",
keywords = "Adolescent, Adult, Celiac Disease/etiology, Child, Child, Preschool, Chromosome Aberrations, Congenital Abnormalities, Female, Heart Defects, Congenital/complications, Humans, Infant, Infant, Newborn, Male, Proportional Hazards Models, Registries, Risk Factors, Siblings, Sweden, Young Adult",
author = "{Clinical Sciences, Malm{\"o}, Lund University}, Department and Daniel Agardh and Lund univers",
year = "2012",
month = dec,
doi = "10.1097/MPG.0b013e318269f19d",
language = "English",
volume = "55",
pages = "736--9",
journal = "Journal of Pediatric Gastroenterology and Nutrition",
issn = "0277-2116",
publisher = "Lippincott Williams & Wilkins",
number = "6",

}

RIS

TY - JOUR

T1 - Congenital anomalies and childhood celiac disease in Sweden

AU - Clinical Sciences, Malmö, Lund University, Department

AU - Agardh, Daniel

AU - univers, Lund

PY - 2012/12

Y1 - 2012/12

N2 - 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 of the 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 face, neck, ear, heart, digestive tract, or chromosomes were associated with CD.

AB - 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 of the 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 face, neck, ear, heart, digestive tract, or chromosomes were associated with CD.

KW - Adolescent

KW - Adult

KW - Celiac Disease/etiology

KW - Child

KW - Child, Preschool

KW - Chromosome Aberrations

KW - Congenital Abnormalities

KW - Female

KW - Heart Defects, Congenital/complications

KW - Humans

KW - Infant

KW - Infant, Newborn

KW - Male

KW - Proportional Hazards Models

KW - Registries

KW - Risk Factors

KW - Siblings

KW - Sweden

KW - Young Adult

U2 - 10.1097/MPG.0b013e318269f19d

DO - 10.1097/MPG.0b013e318269f19d

M3 - Journal article

C2 - 22847461

VL - 55

SP - 736

EP - 739

JO - Journal of Pediatric Gastroenterology and Nutrition

JF - Journal of Pediatric Gastroenterology and Nutrition

SN - 0277-2116

IS - 6

ER -

ID: 364813245