Disease Behavior in Children with Crohn’s Disease: The Effect of Disease Duration, Ethnicity, Genotype, and Phenotype

Ron Shaoul, Amir Karban, +7 authors Arie Levine
Published 2008 in Digestive Diseases and Sciences

Abstract

Background Disease behavior in Crohn’s disease (CD) may be modified by disease location and genotype. Disease behavior may change over time, and thus analysis requires follow-up. To date, there have been few pediatric studies that have evaluated the association between disease behavior and genotype with prolonged follow-up. The aim of our study was to… (More)

DOI: 10.1007/s10620-008-0326-7

ID Arnott, ER Nimmo, +12 authors patients Irish Crohn’s disease
doi:10.1038/sj.gene.6364111 Dig Dis Sci
2009

Disease Behavior in Children with Crohn’s Disease: The Effect of Disease Duration, Ethnicity, Genotype, and Phenotype

Abstract

Topics

6 Figures and Tables

Cited By

NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease.

Higher Morbidity of Monogenic Inflammatory Bowel Disease Compared to the Adolescent Onset Inflammatory Bowel Disease

Clinical and Phenotypic Differences in Inflammatory Bowel Disease Among Arab and Jewish Children in Israel

Crohn’s Strictures—Moving Away from the Knife

Ashkenazi Jewish Origin Protects Against Formation of Antibodies to Infliximab and Therapy Failure

Incidence, outcomes, and health services burden of very early onset inflammatory bowel disease.

Pediatric modification of the Montreal classification for inflammatory bowel disease: the Paris classification.

Prediction of disease complication occurrence in Crohn's disease using phenotype and genotype parameters at diagnosis.

Peyer's Patches: The Immune Sensors of the Intestine

The Montreal classification for Crohn's disease: clinical application to a Brazilian single-center cohort of 90 consecutive patients.

References

Epidemiologic and clinical characteristics of children with newly diagnosed inflammatory bowel disease in Wisconsin: a statewide population-based study.

Genotype-phenotype analysis in childhood-onset Crohn's disease: NOD2/CARD15 variants consistently predict phenotypic characteristics of severe disease.

NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease

Behaviour of Crohn's disease according to the Vienna classification.

evidence for genetic heterogeneity within Europe? Genes Immun 5:417–425

Pediatric onset Crohn's colitis is characterized by genotype-dependent age-related susceptibility.

Risk Factors for Perianal Crohn's Disease: The Role of Genotype, Phenotype, and Ethnicity

A Polymorphism in the TNF-α Promoter Gene is Associated with Pediatric Onset and Colonic Location of Crohn's Disease

CARD15 mutations are rare in Swedish pediatric Crohn disease.

Children with early-onset inflammatory bowel disease (IBD): analysis of a pediatric IBD consortium registry.

Slides referencing similar topics

Disease Behavior in Children with Crohn’s Disease: The Effect of Disease Duration, Ethnicity, Genotype, and Phenotype

Abstract

Topics

6 Figures and Tables

Cited By

NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease.

Higher Morbidity of Monogenic Inflammatory Bowel Disease Compared to the Adolescent Onset Inflammatory Bowel Disease

Clinical and Phenotypic Differences in Inflammatory Bowel Disease Among Arab and Jewish Children in Israel

Crohn’s Strictures—Moving Away from the Knife

Ashkenazi Jewish Origin Protects Against Formation of Antibodies to Infliximab and Therapy Failure

Incidence, outcomes, and health services burden of very early onset inflammatory bowel disease.

Pediatric modification of the Montreal classification for inflammatory bowel disease: the Paris classification.

Prediction of disease complication occurrence in Crohn's disease using phenotype and genotype parameters at diagnosis.

Peyer's Patches: The Immune Sensors of the Intestine

The Montreal classification for Crohn's disease: clinical application to a Brazilian single-center cohort of 90 consecutive patients.

References

Epidemiologic and clinical characteristics of children with newly diagnosed inflammatory bowel disease in Wisconsin: a statewide population-based study.

Genotype-phenotype analysis in childhood-onset Crohn's disease: NOD2/CARD15 variants consistently predict phenotypic characteristics of severe disease.

NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease

Behaviour of Crohn's disease according to the Vienna classification.

evidence for genetic heterogeneity within Europe? Genes Immun 5:417–425

Pediatric onset Crohn's colitis is characterized by genotype-dependent age-related susceptibility.

Risk Factors for Perianal Crohn's Disease: The Role of Genotype, Phenotype, and Ethnicity

A Polymorphism in the TNF-α Promoter Gene is Associated with Pediatric Onset and Colonic Location of Crohn's Disease

CARD15 mutations are rare in Swedish pediatric Crohn disease.

Children with early-onset inflammatory bowel disease (IBD): analysis of a pediatric IBD consortium registry.

Similar Papers

Slides referencing similar topics